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rs397507651

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507651(-;-)
Make rs397507651(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337373
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507651
ebirs397507651
HLIrs397507651
Exacrs397507651
Varsomers397507651
Maprs397507651
PheGenIrs397507651
hapmaprs397507651
1000 genomesrs397507651
hgdprs397507651
ensemblrs397507651
gopubmedrs397507651
geneviewrs397507651
scholarrs397507651
googlers397507651
pharmgkbrs397507651
gwascentralrs397507651
openSNPrs397507651
23andMers397507651
23andMe allrs397507651
SNP Nexus

SNPshotrs397507651
SNPdbers397507651
MSV3drs397507651
GWAS Ctlgrs397507651
Max Magnitude0
ClinVar
Risk rs397507651(;)
Alt rs397507651(;)
Reference rs397507651(A;A)
Significance Pathogenic
Disease Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32911510delA
CLNSRC ClinVar
CLNACC RCV000044104.2, RCV000221234.1,