chr8:127705823:G>T Detail (hg38)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr8:128,718,068-128,718,068 View the variant detail on this assembly version. |
hg38 | chr8:127,705,823-127,705,823 |
HGVS
[No Data.]
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.301 | |
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 |
---|---|---|---|---|---|
0.129 | Malignant neoplasm of urinary bladder | Three previously established bladder cancer risk-associated SNPs (rs798766 in TA... | BeFree | 24155119 | Detail |
<0.001 | Carcinoma of bladder | Three previously established bladder cancer risk-associated SNPs (rs798766 in TA... | BeFree | 24155119 | Detail |
0.004 | Carcinoma of bladder | Three previously established bladder cancer risk-associated SNPs (rs798766 in TA... | BeFree | 24155119 | Detail |
0.123 | Malignant neoplasm of urinary bladder | Three previously established bladder cancer risk-associated SNPs (rs798766 in TA... | BeFree | 24155119 | Detail |
0.003 | Carcinoma of bladder | We genotyped rs9642880 G>T on 8q24 and rs710521 A>G on 3q28 in a two-stage... | BeFree | 19369583 | Detail |
0.008 | Malignant neoplasm of urinary bladder | We genotyped rs9642880 G>T on 8q24 and rs710521 A>G on 3q28 in a two-stage... | BeFree | 19369583 | Detail |
0.003 | Carcinoma of bladder | Recently, a genome-wide single nucleotide polymorphism association study has ide... | BeFree | 19801959 | Detail |
0.008 | Malignant neoplasm of urinary bladder | [Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.] | GAD | 18794855 | Detail |
0.007 | Bladder Neoplasm | [A multi-stage genome-wide association study of bladder cancer identifies multip... | GAD | 20972438 | Detail |
0.107 | Malignant neoplasm of urinary bladder | [Susceptibility to urinary bladder cancer: relevance of rs9642880T, GSTM1 0/0 an... | GAD | 19801959 | Detail |
0.027 | Carcinoma of bladder | Therefore, the degree to which rs9642880[T] and GSTM1 0/0 confer susceptibility ... | BeFree | 19801959 | Detail |
0.107 | Malignant neoplasm of urinary bladder | Therefore, the degree to which rs9642880[T] and GSTM1 0/0 confer susceptibility ... | BeFree | 19801959 | Detail |
0.008 | Malignant neoplasm of urinary bladder | Recently, a genome-wide single nucleotide polymorphism association study has ide... | BeFree | 19801959 | Detail |
0.007 | Bladder Neoplasm | [Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.] | GAD | 18794855 | Detail |
0.007 | Bladder Neoplasm | [A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.] | GAD | 20348956 | Detail |
0.027 | Carcinoma of bladder | These findings suggest that seven bladder cancer risk-associated variants (rs964... | BeFree | 24740636 | Detail |
0.107 | Malignant neoplasm of urinary bladder | These findings suggest that seven bladder cancer risk-associated variants (rs964... | BeFree | 24740636 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Three previously established bladder cancer risk-associated SNPs (rs798766 in TACC3, rs9642880 in MY... | DisGeNET | Detail |
Three previously established bladder cancer risk-associated SNPs (rs798766 in TACC3, rs9642880 in MY... | DisGeNET | Detail |
Three previously established bladder cancer risk-associated SNPs (rs798766 in TACC3, rs9642880 in MY... | DisGeNET | Detail |
Three previously established bladder cancer risk-associated SNPs (rs798766 in TACC3, rs9642880 in MY... | DisGeNET | Detail |
We genotyped rs9642880 G>T on 8q24 and rs710521 A>G on 3q28 in a two-stage case-control study ... | DisGeNET | Detail |
We genotyped rs9642880 G>T on 8q24 and rs710521 A>G on 3q28 in a two-stage case-control study ... | DisGeNET | Detail |
Recently, a genome-wide single nucleotide polymorphism association study has identified a sequence v... | DisGeNET | Detail |
[Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.] | DisGeNET | Detail |
[A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility lo... | DisGeNET | Detail |
[Susceptibility to urinary bladder cancer: relevance of rs9642880T, GSTM1 0/0 and occupational expos... | DisGeNET | Detail |
Therefore, the degree to which rs9642880[T] and GSTM1 0/0 confer susceptibility to urinary bladder c... | DisGeNET | Detail |
Therefore, the degree to which rs9642880[T] and GSTM1 0/0 confer susceptibility to urinary bladder c... | DisGeNET | Detail |
Recently, a genome-wide single nucleotide polymorphism association study has identified a sequence v... | DisGeNET | Detail |
[Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.] | DisGeNET | Detail |
[A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.] | DisGeNET | Detail |
These findings suggest that seven bladder cancer risk-associated variants (rs9642880, rs2294008, rs7... | DisGeNET | Detail |
These findings suggest that seven bladder cancer risk-associated variants (rs9642880, rs2294008, rs7... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs9642880 dbSNP
- Genome
- hg38
- Position
- chr8:127,705,823-127,705,823
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
- 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))
- rs9642880
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.3012
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 5048
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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