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rs397509276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509276(-;-)
Make rs397509276(-;T)
Make rs397509276(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43049140
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509276
ebirs397509276
HLIrs397509276
Exacrs397509276
Varsomers397509276
Maprs397509276
PheGenIrs397509276
hapmaprs397509276
1000 genomesrs397509276
hgdprs397509276
ensemblrs397509276
gopubmedrs397509276
geneviewrs397509276
scholarrs397509276
googlers397509276
pharmgkbrs397509276
gwascentralrs397509276
openSNPrs397509276
23andMers397509276
23andMe allrs397509276
SNP Nexus

SNPshotrs397509276
SNPdbers397509276
MSV3drs397509276
GWAS Ctlgrs397509276
Max Magnitude0
ClinVar
Risk rs397509276(T;T)
Alt rs397509276(T;T)
Reference rs397509276(;)
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.41201158dupA
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048969.2, RCV000112631.1,