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rs398122796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122796(-;-)
Make rs398122796(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339570
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122796
ebirs398122796
HLIrs398122796
Exacrs398122796
Varsomers398122796
Maprs398122796
PheGenIrs398122796
hapmaprs398122796
1000 genomesrs398122796
hgdprs398122796
ensemblrs398122796
gopubmedrs398122796
geneviewrs398122796
scholarrs398122796
googlers398122796
pharmgkbrs398122796
gwascentralrs398122796
openSNPrs398122796
23andMers398122796
23andMe allrs398122796
SNP Nexus

SNPshotrs398122796
SNPdbers398122796
MSV3drs398122796
GWAS Ctlgrs398122796
Max Magnitude0
ClinVar
Risk rs398122796(;)
Alt rs398122796(;)
Reference rs398122796(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.32913707delT
CLNSRC ClinVar
CLNACC RCV000077747.2,