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rs398122601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122601(-;-)
Make rs398122601(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363510
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122601
ebirs398122601
HLIrs398122601
Exacrs398122601
Varsomers398122601
Maprs398122601
PheGenIrs398122601
hapmaprs398122601
1000 genomesrs398122601
hgdprs398122601
ensemblrs398122601
gopubmedrs398122601
geneviewrs398122601
scholarrs398122601
googlers398122601
pharmgkbrs398122601
gwascentralrs398122601
openSNPrs398122601
23andMers398122601
23andMe allrs398122601
SNP Nexus

SNPshotrs398122601
SNPdbers398122601
MSV3drs398122601
GWAS Ctlgrs398122601
Max Magnitude0
ClinVar
Risk rs398122601(;)
Alt rs398122601(;)
Reference rs398122601(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32937647delG
CLNSRC ClinVar
CLNACC RCV000077023.2, RCV000216064.1,