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rs397509195

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509195(C;G)
Make rs397509195(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071154
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509195
ebirs397509195
HLIrs397509195
Exacrs397509195
Varsomers397509195
Maprs397509195
PheGenIrs397509195
hapmaprs397509195
1000 genomesrs397509195
hgdprs397509195
ensemblrs397509195
gopubmedrs397509195
geneviewrs397509195
scholarrs397509195
googlers397509195
pharmgkbrs397509195
gwascentralrs397509195
openSNPrs397509195
23andMers397509195
23andMe allrs397509195
SNP Nexus

SNPshotrs397509195
SNPdbers397509195
MSV3drs397509195
GWAS Ctlgrs397509195
Max Magnitude0
ClinVar
Risk rs397509195(G;G)
Alt rs397509195(G;G)
Reference rs397509195(C;C)
Significance Pathogenic
Disease Familial cancer of breast not provided Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast not provided Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41223171G>C
CLNSRC ClinVar
CLNACC RCV000048653.2, RCV000236263.1, RCV000238826.1,