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rs397508991

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common/normal
(-;G) 6 BRCA1 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar
Make rs397508991(-;A)
Make rs397508991(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092871
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508991
dbSNP (old)rs397508991
ClinGenrs397508991
ebirs397508991
HLIrs397508991
Exacrs397508991
Gnomadrs397508991
Varsomers397508991
Maprs397508991
PheGenIrs397508991
Biobankrs397508991
1000 genomesrs397508991
hgdprs397508991
ensemblrs397508991
gopubmedrs397508991
geneviewrs397508991
scholarrs397508991
googlers397508991
pharmgkbrs397508991
gwascentralrs397508991
openSNPrs397508991
23andMers397508991
23andMe allrs397508991
SNP Nexus

SNPshotrs397508991
SNPdbers397508991
MSV3drs397508991
GWAS Ctlgrs397508991
Max Magnitude6
ClinVar
Risk rs397508991(A;A) rs397508991(G;G)
Alt rs397508991(A;A) rs397508991(G;G)
Reference Rs397508991(-;-)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244889dupC
CLNSRC ClinVar
CLNACC RCV000047913.2, RCV000256855.2,