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rs375064902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs375064902(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340210
GeneBRCA2
is asnp
is mentioned by
dbSNPrs375064902
dbSNP (old)rs375064902
ClinGenrs375064902
ebirs375064902
HLIrs375064902
Exacrs375064902
Gnomadrs375064902
Varsomers375064902
Maprs375064902
PheGenIrs375064902
Biobankrs375064902
1000 genomesrs375064902
hgdprs375064902
ensemblrs375064902
gopubmedrs375064902
geneviewrs375064902
scholarrs375064902
googlers375064902
pharmgkbrs375064902
gwascentralrs375064902
openSNPrs375064902
23andMers375064902
23andMe allrs375064902
SNP Nexus

SNPshotrs375064902
SNPdbers375064902
MSV3drs375064902
GWAS Ctlgrs375064902
Max Magnitude6
ClinVar
Risk rs375064902(A;A) rs375064902(G;G)
Alt rs375064902(A;A) rs375064902(G;G)
Reference Rs375064902(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32914347T>A; NC_000013.10:g.32914347T>G
CLNSRC ClinVar
CLNACC RCV000031583.6, RCV000149889.2, RCV000082952.2,