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rs398122608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122608(A;T)
Make rs398122608(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371049
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122608
ebirs398122608
HLIrs398122608
Exacrs398122608
Varsomers398122608
Maprs398122608
PheGenIrs398122608
hapmaprs398122608
1000 genomesrs398122608
hgdprs398122608
ensemblrs398122608
gopubmedrs398122608
geneviewrs398122608
scholarrs398122608
googlers398122608
pharmgkbrs398122608
gwascentralrs398122608
openSNPrs398122608
23andMers398122608
23andMe allrs398122608
SNP Nexus

SNPshotrs398122608
SNPdbers398122608
MSV3drs398122608
GWAS Ctlgrs398122608
Max Magnitude0
ClinVar
Risk rs398122608(T;T)
Alt rs398122608(T;T)
Reference rs398122608(A;A)
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.32945186A>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000077032.2, RCV000130528.2,