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rs397508928

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508928(-;-)
Make rs397508928(-;GT)
Make rs397508928(GT;GT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093517
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508928
ebirs397508928
HLIrs397508928
Exacrs397508928
Varsomers397508928
Maprs397508928
PheGenIrs397508928
hapmaprs397508928
1000 genomesrs397508928
hgdprs397508928
ensemblrs397508928
gopubmedrs397508928
geneviewrs397508928
scholarrs397508928
googlers397508928
pharmgkbrs397508928
gwascentralrs397508928
openSNPrs397508928
23andMers397508928
23andMe allrs397508928
SNP Nexus

SNPshotrs397508928
SNPdbers397508928
MSV3drs397508928
GWAS Ctlgrs397508928
Max Magnitude0
ClinVar
Risk rs397508928(GT;GT)
Alt rs397508928(GT;GT)
Reference rs397508928(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245535_41245536dupAC
CLNSRC ClinVar
CLNACC RCV000047681.2,