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rs398122737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122737(-;-)
Make rs398122737(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336380
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122737
ebirs398122737
HLIrs398122737
Exacrs398122737
Varsomers398122737
Maprs398122737
PheGenIrs398122737
hapmaprs398122737
1000 genomesrs398122737
hgdprs398122737
ensemblrs398122737
gopubmedrs398122737
geneviewrs398122737
scholarrs398122737
googlers398122737
pharmgkbrs398122737
gwascentralrs398122737
openSNPrs398122737
23andMers398122737
23andMe allrs398122737
SNP Nexus

SNPshotrs398122737
SNPdbers398122737
MSV3drs398122737
GWAS Ctlgrs398122737
Max Magnitude0
ClinVar
Risk rs398122737(;)
Alt rs398122737(;)
Reference rs398122737(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.32910517delA
CLNSRC ClinVar
CLNACC RCV000077674.2,