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rs397509015

From SNPedia

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


Make rs397509015(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092696
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509015
dbSNP (old)rs397509015
ClinGenrs397509015
ebirs397509015
HLIrs397509015
Exacrs397509015
Gnomadrs397509015
Varsomers397509015
Maprs397509015
PheGenIrs397509015
Biobankrs397509015
1000 genomesrs397509015
hgdprs397509015
ensemblrs397509015
gopubmedrs397509015
geneviewrs397509015
scholarrs397509015
googlers397509015
pharmgkbrs397509015
gwascentralrs397509015
openSNPrs397509015
23andMers397509015
23andMe allrs397509015
SNP Nexus

SNPshotrs397509015
SNPdbers397509015
MSV3drs397509015
GWAS Ctlgrs397509015
Max Magnitude6
ClinVar
Risk rs397509015(-;-)
Alt rs397509015(-;-)
Reference Rs397509015(GT;GT)
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.41244713_41244714delAC
CLNSRC ClinVar
CLNACC RCV000047983.2, RCV000256970.1,