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rs397509187

From SNPedia

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


Make rs397509187(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071233
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509187
ClinGenrs397509187
ebirs397509187
HLIrs397509187
Exacrs397509187
Varsomers397509187
Maprs397509187
PheGenIrs397509187
hapmaprs397509187
1000 genomesrs397509187
hgdprs397509187
ensemblrs397509187
gopubmedrs397509187
geneviewrs397509187
scholarrs397509187
googlers397509187
pharmgkbrs397509187
gwascentralrs397509187
openSNPrs397509187
23andMers397509187
23andMe allrs397509187
SNP Nexus

SNPshotrs397509187
SNPdbers397509187
MSV3drs397509187
GWAS Ctlgrs397509187
Max Magnitude6
ClinVar
Risk rs397509187(-;-)
Alt rs397509187(-;-)
Reference Rs397509187(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.41223250delT
CLNSRC ClinVar
CLNACC RCV000048627.2, RCV000257350.2,