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rs398122763

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122763(-;-)
Make rs398122763(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337691
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122763
ebirs398122763
HLIrs398122763
Exacrs398122763
Varsomers398122763
Maprs398122763
PheGenIrs398122763
hapmaprs398122763
1000 genomesrs398122763
hgdprs398122763
ensemblrs398122763
gopubmedrs398122763
geneviewrs398122763
scholarrs398122763
googlers398122763
pharmgkbrs398122763
gwascentralrs398122763
openSNPrs398122763
23andMers398122763
23andMe allrs398122763
SNP Nexus

SNPshotrs398122763
SNPdbers398122763
MSV3drs398122763
GWAS Ctlgrs398122763
Max Magnitude0
ClinVar
Risk rs398122763(;)
Alt rs398122763(;)
Reference rs398122763(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911828delA
CLNSRC ClinVar
CLNACC RCV000077706.2,