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rs398122617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122617(A;A)
Make rs398122617(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32396969
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122617
ebirs398122617
HLIrs398122617
Exacrs398122617
Varsomers398122617
Maprs398122617
PheGenIrs398122617
hapmaprs398122617
1000 genomesrs398122617
hgdprs398122617
ensemblrs398122617
gopubmedrs398122617
geneviewrs398122617
scholarrs398122617
googlers398122617
pharmgkbrs398122617
gwascentralrs398122617
openSNPrs398122617
23andMers398122617
23andMe allrs398122617
SNP Nexus

SNPshotrs398122617
SNPdbers398122617
MSV3drs398122617
GWAS Ctlgrs398122617
Max Magnitude0
ClinVar
Risk rs398122617(A;A)
Alt rs398122617(A;A)
Reference rs398122617(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32971106G>A
CLNSRC ClinVar
CLNACC RCV000077046.2,