chr8:35741644:A>G Detail (hg19)

Information

Genome

Assembly Position
hg19 chr8:35,741,644-35,741,644
hg38 chr8:35,884,126-35,884,126 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

[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
0.022 Malignant neoplasm of breast Seven single nucleotide polymorphisms (SNPs) (rs3856806 in PPARG, rs7014346 in P... BeFree 24338422 Detail
0.008 breast carcinoma Seven single nucleotide polymorphisms (SNPs) (rs3856806 in PPARG, rs7014346 in P... BeFree 24338422 Detail
0.127 Malignant neoplasm of breast Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN... BeFree 24338422 Detail
0.001 breast carcinoma Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN... BeFree 24338422 Detail
0.004 breast carcinoma Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN... BeFree 24338422 Detail
0.001 Malignant neoplasm of breast Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN... BeFree 24338422 Detail
Annotation

Annotations

DescrptionSourceLinks
Seven single nucleotide polymorphisms (SNPs) (rs3856806 in PPARG, rs7014346 in POU5F1P1, rs989902 in... DisGeNET Detail
Seven single nucleotide polymorphisms (SNPs) (rs3856806 in PPARG, rs7014346 in POU5F1P1, rs989902 in... DisGeNET Detail
Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN13, and rs7003146 in... DisGeNET Detail
Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN13, and rs7003146 in... DisGeNET Detail
Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN13, and rs7003146 in... DisGeNET Detail
Our results confirmed the association of rs7014346 in POU5F1P1, rs989902 in PTPN13, and rs7003146 in... DisGeNET Detail
Gene
-
dbSNP
rs7003146 dbSNP
Genome
hg19
Position
chr8:35,741,644-35,741,644
Variant Type
snv
Reference Allele
A
Alternative Allele
G
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