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rs398122715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122715(G;T)
Make rs398122715(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379401
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122715
ebirs398122715
HLIrs398122715
Exacrs398122715
Varsomers398122715
Maprs398122715
PheGenIrs398122715
hapmaprs398122715
1000 genomesrs398122715
hgdprs398122715
ensemblrs398122715
gopubmedrs398122715
geneviewrs398122715
scholarrs398122715
googlers398122715
pharmgkbrs398122715
gwascentralrs398122715
openSNPrs398122715
23andMers398122715
23andMe allrs398122715
SNP Nexus

SNPshotrs398122715
SNPdbers398122715
MSV3drs398122715
GWAS Ctlgrs398122715
Max Magnitude0
ClinVar
Risk rs398122715(T;T)
Alt rs398122715(T;T)
Reference rs398122715(G;G)
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.32953538G>T
CLNSRC ClinVar
CLNACC RCV000077644.2, RCV000198305.2,