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rs397509264

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509264(A;C)
Make rs397509264(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049196
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509264
dbSNP (old)rs397509264
ClinGenrs397509264
ebirs397509264
HLIrs397509264
Exacrs397509264
Gnomadrs397509264
Varsomers397509264
Maprs397509264
PheGenIrs397509264
Biobankrs397509264
1000 genomesrs397509264
hgdprs397509264
ensemblrs397509264
gopubmedrs397509264
geneviewrs397509264
scholarrs397509264
googlers397509264
pharmgkbrs397509264
gwascentralrs397509264
openSNPrs397509264
23andMers397509264
23andMe allrs397509264
SNP Nexus

SNPshotrs397509264
SNPdbers397509264
MSV3drs397509264
GWAS Ctlgrs397509264
Max Magnitude0
ClinVar
Risk rs397509264(C;C) rs397509264(T;T)
Alt rs397509264(C;C) rs397509264(T;T)
Reference Rs397509264(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.41201213T>A; NC_000017.10:g.41201213T>G
CLNSRC ClinVar
CLNACC RCV000048942.2, RCV000077616.2, RCV000048941.2, RCV000258161.1,