Have questions? Visit https://www.reddit.com/r/SNPedia

rs398122557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122557(-;-)
Make rs398122557(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340799
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122557
ebirs398122557
HLIrs398122557
Exacrs398122557
Varsomers398122557
Maprs398122557
PheGenIrs398122557
hapmaprs398122557
1000 genomesrs398122557
hgdprs398122557
ensemblrs398122557
gopubmedrs398122557
geneviewrs398122557
scholarrs398122557
googlers398122557
pharmgkbrs398122557
gwascentralrs398122557
openSNPrs398122557
23andMers398122557
23andMe allrs398122557
SNP Nexus

SNPshotrs398122557
SNPdbers398122557
MSV3drs398122557
GWAS Ctlgrs398122557
Max Magnitude0
ClinVar
Risk rs398122557(;)
Alt rs398122557(;)
Reference rs398122557(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914936delT
CLNSRC ClinVar
CLNACC RCV000076966.2,