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rs398122711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122711(A;A)
Make rs398122711(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32376669
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122711
ebirs398122711
HLIrs398122711
Exacrs398122711
Varsomers398122711
Maprs398122711
PheGenIrs398122711
hapmaprs398122711
1000 genomesrs398122711
hgdprs398122711
ensemblrs398122711
gopubmedrs398122711
geneviewrs398122711
scholarrs398122711
googlers398122711
pharmgkbrs398122711
gwascentralrs398122711
openSNPrs398122711
23andMers398122711
23andMe allrs398122711
SNP Nexus

SNPshotrs398122711
SNPdbers398122711
MSV3drs398122711
GWAS Ctlgrs398122711
Max Magnitude0
ClinVar
Risk rs398122711(A;A)
Alt rs398122711(A;A)
Reference rs398122711(G;G)
Significance Other
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32950806G>A
CLNSRC ClinVar
CLNACC RCV000077639.2,