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rs397507960

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507960(C;T)
Make rs397507960(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363258
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507960
ebirs397507960
HLIrs397507960
Exacrs397507960
Varsomers397507960
Maprs397507960
PheGenIrs397507960
hapmaprs397507960
1000 genomesrs397507960
hgdprs397507960
ensemblrs397507960
gopubmedrs397507960
geneviewrs397507960
scholarrs397507960
googlers397507960
pharmgkbrs397507960
gwascentralrs397507960
openSNPrs397507960
23andMers397507960
23andMe allrs397507960
SNP Nexus

SNPshotrs397507960
SNPdbers397507960
MSV3drs397507960
GWAS Ctlgrs397507960
Max Magnitude0
ClinVar
Risk rs397507960(T;T)
Alt rs397507960(T;T)
Reference rs397507960(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.32937395C>T
CLNSRC ClinVar
CLNACC RCV000045404.2,