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rs398122602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122602(A;A)
Make rs398122602(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363535
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122602
ebirs398122602
HLIrs398122602
Exacrs398122602
Varsomers398122602
Maprs398122602
PheGenIrs398122602
hapmaprs398122602
1000 genomesrs398122602
hgdprs398122602
ensemblrs398122602
gopubmedrs398122602
geneviewrs398122602
scholarrs398122602
googlers398122602
pharmgkbrs398122602
gwascentralrs398122602
openSNPrs398122602
23andMers398122602
23andMe allrs398122602
SNP Nexus

SNPshotrs398122602
SNPdbers398122602
MSV3drs398122602
GWAS Ctlgrs398122602
Max Magnitude0
ClinVar
Risk rs398122602(A;A)
Alt rs398122602(A;A)
Reference rs398122602(T;T)
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.32937672T>A; NC_000013.10:g.32937672T>G
CLNSRC ClinVar
CLNACC RCV000077024.2, RCV000217152.1,