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rs397509038

From SNPedia

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


Make rs397509038(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092386
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509038
dbSNP (old)rs397509038
ClinGenrs397509038
ebirs397509038
HLIrs397509038
Exacrs397509038
Gnomadrs397509038
Varsomers397509038
Maprs397509038
PheGenIrs397509038
Biobankrs397509038
1000 genomesrs397509038
hgdprs397509038
ensemblrs397509038
gopubmedrs397509038
geneviewrs397509038
scholarrs397509038
googlers397509038
pharmgkbrs397509038
gwascentralrs397509038
openSNPrs397509038
23andMers397509038
23andMe allrs397509038
SNP Nexus

SNPshotrs397509038
SNPdbers397509038
MSV3drs397509038
GWAS Ctlgrs397509038
Max Magnitude6
ClinVar
Risk rs397509038(-;-)
Alt rs397509038(-;-)
Reference Rs397509038(T;T)
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.41244403delA
CLNSRC ClinVar
CLNACC RCV000048082.2, RCV000256523.2,