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rs397509256

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509256(G;T)
Make rs397509256(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051102
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509256
ebirs397509256
HLIrs397509256
Exacrs397509256
Varsomers397509256
Maprs397509256
PheGenIrs397509256
hapmaprs397509256
1000 genomesrs397509256
hgdprs397509256
ensemblrs397509256
gopubmedrs397509256
geneviewrs397509256
scholarrs397509256
googlers397509256
pharmgkbrs397509256
gwascentralrs397509256
openSNPrs397509256
23andMers397509256
23andMe allrs397509256
SNP Nexus

SNPshotrs397509256
SNPdbers397509256
MSV3drs397509256
GWAS Ctlgrs397509256
Max Magnitude0
ClinVar
Risk rs397509256(T;T)
Alt rs397509256(T;T)
Reference rs397509256(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.41203119C>A
CLNSRC ClinVar
CLNACC RCV000048914.2,