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rs397507966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507966(C;T)
Make rs397507966(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363393
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507966
ebirs397507966
HLIrs397507966
Exacrs397507966
Varsomers397507966
Maprs397507966
PheGenIrs397507966
hapmaprs397507966
1000 genomesrs397507966
hgdprs397507966
ensemblrs397507966
gopubmedrs397507966
geneviewrs397507966
scholarrs397507966
googlers397507966
pharmgkbrs397507966
gwascentralrs397507966
openSNPrs397507966
23andMers397507966
23andMe allrs397507966
SNP Nexus

SNPshotrs397507966
SNPdbers397507966
MSV3drs397507966
GWAS Ctlgrs397507966
Max Magnitude0
ClinVar
Risk rs397507966(G,T;G,T)
Alt rs397507966(G,T;G,T)
Reference rs397507966(C;C)
Significance Untested
Disease Hereditary breast and ovarian cancer syndrome Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32937530C>G; NC_000013.10:g.32937530C>T
CLNSRC ClinVar
CLNACC RCV000225930.1, RCV000045449.2,