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rs397507884

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507884(A;G)
Make rs397507884(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32329496
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507884
ebirs397507884
HLIrs397507884
Exacrs397507884
Varsomers397507884
Maprs397507884
PheGenIrs397507884
hapmaprs397507884
1000 genomesrs397507884
hgdprs397507884
ensemblrs397507884
gopubmedrs397507884
geneviewrs397507884
scholarrs397507884
googlers397507884
pharmgkbrs397507884
gwascentralrs397507884
openSNPrs397507884
23andMers397507884
23andMe allrs397507884
SNP Nexus

SNPshotrs397507884
SNPdbers397507884
MSV3drs397507884
GWAS Ctlgrs397507884
Max Magnitude0
ClinVar
Risk rs397507884(G;G)
Alt rs397507884(G;G)
Reference rs397507884(A;A)
Significance Untested
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.32903633A>G; NC_000013.10:g.32903633A>T
CLNSRC ClinVar
CLNACC RCV000045057.2, RCV000222207.1,