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rs397509176

From SNPedia

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


Make rs397509176(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43076537
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509176
ClinGenrs397509176
ebirs397509176
HLIrs397509176
Exacrs397509176
Varsomers397509176
Maprs397509176
PheGenIrs397509176
hapmaprs397509176
1000 genomesrs397509176
hgdprs397509176
ensemblrs397509176
gopubmedrs397509176
geneviewrs397509176
scholarrs397509176
googlers397509176
pharmgkbrs397509176
gwascentralrs397509176
openSNPrs397509176
23andMers397509176
23andMe allrs397509176
SNP Nexus

SNPshotrs397509176
SNPdbers397509176
MSV3drs397509176
GWAS Ctlgrs397509176
Max Magnitude6
ClinVar
Risk rs397509176(-;-)
Alt rs397509176(-;-)
Reference Rs397509176(G;G)
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.41228554delC
CLNSRC ClinVar
CLNACC RCV000048559.2, RCV000241018.1,