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rs397509173

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;T) 6 BRCA1 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar
Make rs397509173(A;A)
Make rs397509173(A;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104120
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509173
dbSNP (old)rs397509173
ClinGenrs397509173
ebirs397509173
HLIrs397509173
Exacrs397509173
Gnomadrs397509173
Varsomers397509173
Maprs397509173
PheGenIrs397509173
Biobankrs397509173
1000 genomesrs397509173
hgdprs397509173
ensemblrs397509173
gopubmedrs397509173
geneviewrs397509173
scholarrs397509173
googlers397509173
pharmgkbrs397509173
gwascentralrs397509173
openSNPrs397509173
23andMers397509173
23andMe allrs397509173
SNP Nexus

SNPshotrs397509173
SNPdbers397509173
MSV3drs397509173
GWAS Ctlgrs397509173
Max Magnitude6
ClinVar
Risk rs397509173(A;A) rs397509173(G;G)
Alt rs397509173(A;A) rs397509173(G;G)
Reference Rs397509173(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast Neoplasm of breast
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Familial cancer of breast Neoplasm of breast
Reversed 1
HGVS NC_000017.10:g.41256137A>C; NC_000017.10:g.41256137A>T
CLNSRC ClinVar
CLNACC RCV000225534.2, RCV000048556.2, RCV000414341.1,