chr8:128485038:A>C Detail (hg19)

Information

Genome

Assembly Position
hg19 chr8:128,485,038-128,485,038
hg38 chr8:127,472,793-127,472,793 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:0.831
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
0.003 age related macular degeneration We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.120 Malignant neoplasm of prostate Genome-wide association and replication studies identify four variants associate... GWASCAT 19767754 Detail
0.019 Prostatic Neoplasms [Genome-wide association and replication studies identify four variants associat... GAD 19767754 Detail
0.016 atherosclerosis We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.020 Malignant neoplasm of prostate Forty-nine tagging SNPs including three previously reported significant variants... BeFree 19562729 Detail
0.002 arteriosclerosis We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.001 arteriosclerosis We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.120 Malignant neoplasm of prostate Genome-wide association study identifies a second prostate cancer susceptibility... GWASCAT 17401366 Detail
0.480 age related macular degeneration We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.120 Malignant neoplasm of prostate Genome-wide association study of prostate cancer identifies a second risk locus ... GWASCAT 17401363 Detail
0.019 Prostatic Neoplasms [Genome-wide association study identifies a second prostate cancer susceptibilit... GAD 17401366 Detail
0.011 atherosclerosis We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.002 arteriosclerosis We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.404 age related macular degeneration We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.011 atherosclerosis We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.011 atherosclerosis We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.019 Prostatic Neoplasms [Genome-wide association study of prostate cancer identifies a second risk locus... GAD 17401363 Detail
0.001 arteriosclerosis We investigated the prevalence of common polymorphisms that have been associated... BeFree 18248681 Detail
0.120 Malignant neoplasm of prostate Genetic variation in prostate-specific antigen-detected prostate cancer and the ... GWASCAT 24753544 Detail
0.012 prostate carcinoma Forty-nine tagging SNPs including three previously reported significant variants... BeFree 19562729 Detail
Annotation

Annotations

DescrptionSourceLinks
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
Genome-wide association and replication studies identify four variants associated with prostate canc... DisGeNET Detail
[Genome-wide association and replication studies identify four variants associated with prostate can... DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
Forty-nine tagging SNPs including three previously reported significant variants (rs1447295, rs69832... DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. DisGeNET Detail
[Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.] DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
[Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.] DisGeNET Detail
We investigated the prevalence of common polymorphisms that have been associated with diseases, such... DisGeNET Detail
Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control se... DisGeNET Detail
Forty-nine tagging SNPs including three previously reported significant variants (rs1447295, rs69832... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs1447295 dbSNP
Genome
hg19
Position
chr8:128,485,038-128,485,038
Variant Type
snv
Reference Allele
A
Alternative Allele
C
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))
rs1447295
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.8305
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
13920
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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