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rs397508983

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508983(C;T)
Make rs397508983(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092959
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508983
ebirs397508983
HLIrs397508983
Exacrs397508983
Varsomers397508983
Maprs397508983
PheGenIrs397508983
hapmaprs397508983
1000 genomesrs397508983
hgdprs397508983
ensemblrs397508983
gopubmedrs397508983
geneviewrs397508983
scholarrs397508983
googlers397508983
pharmgkbrs397508983
gwascentralrs397508983
openSNPrs397508983
23andMers397508983
23andMe allrs397508983
SNP Nexus

SNPshotrs397508983
SNPdbers397508983
MSV3drs397508983
GWAS Ctlgrs397508983
Max Magnitude0
ClinVar
Risk rs397508983(T;T)
Alt rs397508983(T;T)
Reference rs397508983(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244976G>A
CLNSRC ClinVar
CLNACC RCV000047885.2,