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rs398122789

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122789(-;-)
Make rs398122789(-;A)
Make rs398122789(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339319
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122789
ebirs398122789
HLIrs398122789
Exacrs398122789
Varsomers398122789
Maprs398122789
PheGenIrs398122789
hapmaprs398122789
1000 genomesrs398122789
hgdprs398122789
ensemblrs398122789
gopubmedrs398122789
geneviewrs398122789
scholarrs398122789
googlers398122789
pharmgkbrs398122789
gwascentralrs398122789
openSNPrs398122789
23andMers398122789
23andMe allrs398122789
SNP Nexus

SNPshotrs398122789
SNPdbers398122789
MSV3drs398122789
GWAS Ctlgrs398122789
Max Magnitude0
ClinVar
Risk rs398122789(A;A)
Alt rs398122789(A;A)
Reference rs398122789(;)
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.32913456dupA
CLNSRC ClinVar
CLNACC RCV000077738.2, RCV000218684.1,