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rs398122565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122565(A;A)
Make rs398122565(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32329493
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122565
ebirs398122565
HLIrs398122565
Exacrs398122565
Varsomers398122565
Maprs398122565
PheGenIrs398122565
hapmaprs398122565
1000 genomesrs398122565
hgdprs398122565
ensemblrs398122565
gopubmedrs398122565
geneviewrs398122565
scholarrs398122565
googlers398122565
pharmgkbrs398122565
gwascentralrs398122565
openSNPrs398122565
23andMers398122565
23andMe allrs398122565
SNP Nexus

SNPshotrs398122565
SNPdbers398122565
MSV3drs398122565
GWAS Ctlgrs398122565
Max Magnitude0
ClinVar
Risk rs398122565(A;A)
Alt rs398122565(A;A)
Reference rs398122565(G;G)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32903630G>A
CLNSRC ClinVar
CLNACC RCV000076974.2,