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rs398122735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122735(C;T)
Make rs398122735(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336300
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122735
ebirs398122735
HLIrs398122735
Exacrs398122735
Varsomers398122735
Maprs398122735
PheGenIrs398122735
hapmaprs398122735
1000 genomesrs398122735
hgdprs398122735
ensemblrs398122735
gopubmedrs398122735
geneviewrs398122735
scholarrs398122735
googlers398122735
pharmgkbrs398122735
gwascentralrs398122735
openSNPrs398122735
23andMers398122735
23andMe allrs398122735
SNP Nexus

SNPshotrs398122735
SNPdbers398122735
MSV3drs398122735
GWAS Ctlgrs398122735
Max Magnitude0
ClinVar
Risk rs398122735(T;T)
Alt rs398122735(T;T)
Reference rs398122735(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910437C>T
CLNSRC ClinVar
CLNACC RCV000077672.2,