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rs397508851

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508851(G;T)
Make rs397508851(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094252
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508851
ebirs397508851
HLIrs397508851
Exacrs397508851
Varsomers397508851
Maprs397508851
PheGenIrs397508851
hapmaprs397508851
1000 genomesrs397508851
hgdprs397508851
ensemblrs397508851
gopubmedrs397508851
geneviewrs397508851
scholarrs397508851
googlers397508851
pharmgkbrs397508851
gwascentralrs397508851
openSNPrs397508851
23andMers397508851
23andMe allrs397508851
SNP Nexus

SNPshotrs397508851
SNPdbers397508851
MSV3drs397508851
GWAS Ctlgrs397508851
Max Magnitude0
ClinVar
Risk rs397508851(T;T)
Alt rs397508851(T;T)
Reference rs397508851(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246269C>A
CLNSRC ClinVar
CLNACC RCV000047403.2,