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rs397508917

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGTA;TGTA) 0 common in clinvar
Make rs397508917(-;-)
Make rs397508917(-;TGTA)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106475
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508917
ebirs397508917
HLIrs397508917
Exacrs397508917
Varsomers397508917
Maprs397508917
PheGenIrs397508917
hapmaprs397508917
1000 genomesrs397508917
hgdprs397508917
ensemblrs397508917
gopubmedrs397508917
geneviewrs397508917
scholarrs397508917
googlers397508917
pharmgkbrs397508917
gwascentralrs397508917
openSNPrs397508917
23andMers397508917
23andMe allrs397508917
SNP Nexus

SNPshotrs397508917
SNPdbers397508917
MSV3drs397508917
GWAS Ctlgrs397508917
Max Magnitude0
ClinVar
Risk rs397508917(;)
Alt rs397508917(;)
Reference rs397508917(TGTA;TGTA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41258492_41258495delTACA
CLNSRC ClinVar
CLNACC RCV000047635.2,