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rs397507667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507667(C;T)
Make rs397507667(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337797
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507667
ebirs397507667
HLIrs397507667
Exacrs397507667
Varsomers397507667
Maprs397507667
PheGenIrs397507667
hapmaprs397507667
1000 genomesrs397507667
hgdprs397507667
ensemblrs397507667
gopubmedrs397507667
geneviewrs397507667
scholarrs397507667
googlers397507667
pharmgkbrs397507667
gwascentralrs397507667
openSNPrs397507667
23andMers397507667
23andMe allrs397507667
SNP Nexus

SNPshotrs397507667
SNPdbers397507667
MSV3drs397507667
GWAS Ctlgrs397507667
Max Magnitude0
ClinVar
Risk rs397507667(T;T)
Alt rs397507667(T;T)
Reference rs397507667(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32911934C>T
CLNSRC ClinVar
CLNACC RCV000044194.2,