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rs397508971

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397508971(-;-)
Make rs397508971(-;TT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093044
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508971
ebirs397508971
HLIrs397508971
Exacrs397508971
Varsomers397508971
Maprs397508971
PheGenIrs397508971
hapmaprs397508971
1000 genomesrs397508971
hgdprs397508971
ensemblrs397508971
gopubmedrs397508971
geneviewrs397508971
scholarrs397508971
googlers397508971
pharmgkbrs397508971
gwascentralrs397508971
openSNPrs397508971
23andMers397508971
23andMe allrs397508971
SNP Nexus

SNPshotrs397508971
SNPdbers397508971
MSV3drs397508971
GWAS Ctlgrs397508971
Max Magnitude0
ClinVar
Risk rs397508971(;)
Alt rs397508971(;)
Reference rs397508971(TT;TT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41245061_41245062delAA
CLNSRC ClinVar
CLNACC RCV000047858.2,