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rs397507982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507982(C;C)
Make rs397507982(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370466
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507982
ebirs397507982
HLIrs397507982
Exacrs397507982
Varsomers397507982
Maprs397507982
PheGenIrs397507982
hapmaprs397507982
1000 genomesrs397507982
hgdprs397507982
ensemblrs397507982
gopubmedrs397507982
geneviewrs397507982
scholarrs397507982
googlers397507982
pharmgkbrs397507982
gwascentralrs397507982
openSNPrs397507982
23andMers397507982
23andMe allrs397507982
SNP Nexus

SNPshotrs397507982
SNPdbers397507982
MSV3drs397507982
GWAS Ctlgrs397507982
Max Magnitude0
ClinVar
Risk rs397507982(C;C)
Alt rs397507982(C;C)
Reference rs397507982(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32944603G>C
CLNSRC ClinVar
CLNACC RCV000045506.2,