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rs397507908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507908(C;T)
Make rs397507908(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355114
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507908
ebirs397507908
HLIrs397507908
Exacrs397507908
Varsomers397507908
Maprs397507908
PheGenIrs397507908
hapmaprs397507908
1000 genomesrs397507908
hgdprs397507908
ensemblrs397507908
gopubmedrs397507908
geneviewrs397507908
scholarrs397507908
googlers397507908
pharmgkbrs397507908
gwascentralrs397507908
openSNPrs397507908
23andMers397507908
23andMe allrs397507908
SNP Nexus

SNPshotrs397507908
SNPdbers397507908
MSV3drs397507908
GWAS Ctlgrs397507908
Max Magnitude0
ClinVar
Risk rs397507908(T;T)
Alt rs397507908(T;T)
Reference rs397507908(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.32929251C>T
CLNSRC ClinVar
CLNACC RCV000045179.2,