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rs398122610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122610(G;T)
Make rs398122610(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380016
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122610
ebirs398122610
HLIrs398122610
Exacrs398122610
Varsomers398122610
Maprs398122610
PheGenIrs398122610
hapmaprs398122610
1000 genomesrs398122610
hgdprs398122610
ensemblrs398122610
gopubmedrs398122610
geneviewrs398122610
scholarrs398122610
googlers398122610
pharmgkbrs398122610
gwascentralrs398122610
openSNPrs398122610
23andMers398122610
23andMe allrs398122610
SNP Nexus

SNPshotrs398122610
SNPdbers398122610
MSV3drs398122610
GWAS Ctlgrs398122610
Max Magnitude0
ClinVar
Risk rs398122610(T;T)
Alt rs398122610(T;T)
Reference rs398122610(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32954153G>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000077034.2, RCV000130444.2,