chr1:121280613:A>G Detail (hg19)

Information

Genome

Assembly Position
hg19 chr1:121,280,613-121,280,613
hg38 chr1:121,538,815-121,538,815 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.027
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Invasive Ductal Breast Carcinoma A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (... BeFree 25120811 Detail
<0.001 Noninfiltrating Intraductal Carcinoma A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (... BeFree 25120811 Detail
<0.001 Noninfiltrating Intraductal Carcinoma A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (... BeFree 25120811 Detail
<0.001 Noninfiltrating Intraductal Carcinoma A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (... BeFree 25120811 Detail
<0.001 Invasive Ductal Breast Carcinoma A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (... BeFree 25120811 Detail
<0.001 Invasive Ductal Breast Carcinoma A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (... BeFree 25120811 Detail
<0.001 breast carcinoma We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.132 Malignant neoplasm of breast We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.001 breast carcinoma We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.001 Malignant neoplasm of breast We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.003 breast carcinoma We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.123 Malignant neoplasm of breast We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.002 breast carcinoma Our results in two independent data sets suggest that rs11249433, which is locat... BeFree 24292867 Detail
0.129 Mammary Neoplasms Our results in two independent data sets suggest that rs11249433, which is locat... BeFree 24292867 Detail
0.120 Malignant neoplasm of breast Large-scale genotyping identifies 41 new loci associated with breast cancer risk... GWASCAT 23535729 Detail
0.003 Malignant neoplasm of breast Our results in two independent data sets suggest that rs11249433, which is locat... BeFree 24292867 Detail
<0.001 breast carcinoma Our results in two independent data sets suggest that rs11249433, which is locat... BeFree 24292867 Detail
0.129 Mammary Neoplasms NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in E... BeFree 20482849 Detail
0.240 Malignant neoplasm of breast In addition, our data indicate that 1p11-rs11249433 polymorphism is involved in ... BeFree 23977306 Detail
0.120 Malignant neoplasm of breast A multistage genome-wide association study in breast cancer identifies two new r... GWASCAT 19330030 Detail
0.080 breast carcinoma In addition, our data indicate that 1p11-rs11249433 polymorphism is involved in ... BeFree 23977306 Detail
0.080 breast carcinoma In addition, our data indicate that 1p11-rs11249433 polymorphism is involved in ... BeFree 23977306 Detail
0.353 Mammary Neoplasms NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in E... BeFree 20482849 Detail
0.080 breast carcinoma A recent genome-wide association study (GWAS) has identified a single nucleotide... BeFree 20482849 Detail
0.004 Malignant neoplasm of breast NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in E... BeFree 20482849 Detail
0.132 Malignant neoplasm of breast In addition, our data indicate that 1p11-rs11249433 polymorphism is involved in ... BeFree 23977306 Detail
0.004 Malignant neoplasm of breast Our results in two independent data sets suggest that rs11249433, which is locat... BeFree 24292867 Detail
0.240 Malignant neoplasm of breast A recent genome-wide association study (GWAS) has identified a single nucleotide... BeFree 20482849 Detail
<0.001 Mammary Neoplasms Our results in two independent data sets suggest that rs11249433, which is locat... BeFree 24292867 Detail
0.002 breast carcinoma NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in E... BeFree 20482849 Detail
Annotation

Annotations

DescrptionSourceLinks
A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (DCIS) patients and 1... DisGeNET Detail
A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (DCIS) patients and 1... DisGeNET Detail
A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (DCIS) patients and 1... DisGeNET Detail
A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (DCIS) patients and 1... DisGeNET Detail
A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (DCIS) patients and 1... DisGeNET Detail
A total of 100 invasive ductal carcinoma (IDC) and 50 ductal carcinoma in situ (DCIS) patients and 1... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
Our results in two independent data sets suggest that rs11249433, which is located between the NOTCH... DisGeNET Detail
Our results in two independent data sets suggest that rs11249433, which is located between the NOTCH... DisGeNET Detail
Large-scale genotyping identifies 41 new loci associated with breast cancer risk. DisGeNET Detail
Our results in two independent data sets suggest that rs11249433, which is located between the NOTCH... DisGeNET Detail
Our results in two independent data sets suggest that rs11249433, which is located between the NOTCH... DisGeNET Detail
NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tu... DisGeNET Detail
In addition, our data indicate that 1p11-rs11249433 polymorphism is involved in BC susceptibility an... DisGeNET Detail
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.... DisGeNET Detail
In addition, our data indicate that 1p11-rs11249433 polymorphism is involved in BC susceptibility an... DisGeNET Detail
In addition, our data indicate that 1p11-rs11249433 polymorphism is involved in BC susceptibility an... DisGeNET Detail
NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tu... DisGeNET Detail
A recent genome-wide association study (GWAS) has identified a single nucleotide polymorphism (SNP) ... DisGeNET Detail
NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tu... DisGeNET Detail
In addition, our data indicate that 1p11-rs11249433 polymorphism is involved in BC susceptibility an... DisGeNET Detail
Our results in two independent data sets suggest that rs11249433, which is located between the NOTCH... DisGeNET Detail
A recent genome-wide association study (GWAS) has identified a single nucleotide polymorphism (SNP) ... DisGeNET Detail
Our results in two independent data sets suggest that rs11249433, which is located between the NOTCH... DisGeNET Detail
NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tu... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs11249433 dbSNP
Genome
hg19
Position
chr1:121,280,613-121,280,613
Variant Type
snv
Reference Allele
A
Alternative Allele
G
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs11249433
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.027
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
453
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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