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rs397509095

From SNPedia

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


Make rs397509095(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091827
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509095
dbSNP (old)rs397509095
ClinGenrs397509095
ebirs397509095
HLIrs397509095
Exacrs397509095
Varsomers397509095
Maprs397509095
PheGenIrs397509095
Biobankrs397509095
1000 genomesrs397509095
hgdprs397509095
ensemblrs397509095
gopubmedrs397509095
geneviewrs397509095
scholarrs397509095
googlers397509095
pharmgkbrs397509095
gwascentralrs397509095
openSNPrs397509095
23andMers397509095
23andMe allrs397509095
SNP Nexus

SNPshotrs397509095
SNPdbers397509095
MSV3drs397509095
GWAS Ctlgrs397509095
Max Magnitude6
ClinVar
Risk rs397509095(-;-)
Alt rs397509095(-;-)
Reference Rs397509095(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.41243844delT
CLNSRC ClinVar
CLNACC RCV000048289.2, RCV000257069.2,