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rs397508911

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;A) 6 BRCA1 variant considered pathogenic for breast cancer
(A;A) 0 common in clinvar


Make rs397508911(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093708
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508911
dbSNP (old)rs397508911
ClinGenrs397508911
ebirs397508911
HLIrs397508911
Exacrs397508911
Gnomadrs397508911
Varsomers397508911
Maprs397508911
PheGenIrs397508911
Biobankrs397508911
1000 genomesrs397508911
hgdprs397508911
ensemblrs397508911
gopubmedrs397508911
geneviewrs397508911
scholarrs397508911
googlers397508911
pharmgkbrs397508911
gwascentralrs397508911
openSNPrs397508911
23andMers397508911
23andMe allrs397508911
SNP Nexus

SNPshotrs397508911
SNPdbers397508911
MSV3drs397508911
GWAS Ctlgrs397508911
Max Magnitude6
ClinVar
Risk rs397508911(-;-)
Alt rs397508911(-;-)
Reference Rs397508911(A;A)
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.41245725delT
CLNSRC ClinVar
CLNACC RCV000047599.2, RCV000256625.2,