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rs397507275

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507275(A;G)
Make rs397507275(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32333234
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507275
ebirs397507275
HLIrs397507275
Exacrs397507275
Varsomers397507275
Maprs397507275
PheGenIrs397507275
hapmaprs397507275
1000 genomesrs397507275
hgdprs397507275
ensemblrs397507275
gopubmedrs397507275
geneviewrs397507275
scholarrs397507275
googlers397507275
pharmgkbrs397507275
gwascentralrs397507275
openSNPrs397507275
23andMers397507275
23andMe allrs397507275
SNP Nexus

SNPshotrs397507275
SNPdbers397507275
MSV3drs397507275
GWAS Ctlgrs397507275
Max Magnitude0
ClinVar
Risk rs397507275(G;G)
Alt rs397507275(G;G)
Reference rs397507275(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32907371A>G; NC_000013.10:g.32907371A>T
CLNSRC
CLNACC RCV000031336.3, RCV000166903.1, RCV000219960.1,