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rs397509210

From SNPedia

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


Make rs397509210(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43070926
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509210
dbSNP (classic)rs397509210
ClinGenrs397509210
ebirs397509210
HLIrs397509210
Exacrs397509210
Gnomadrs397509210
Varsomers397509210
LitVarrs397509210
Maprs397509210
PheGenIrs397509210
Biobankrs397509210
1000 genomesrs397509210
hgdprs397509210
ensemblrs397509210
geneviewrs397509210
scholarrs397509210
googlers397509210
pharmgkbrs397509210
gwascentralrs397509210
openSNPrs397509210
23andMers397509210
SNPshotrs397509210
SNPdbers397509210
MSV3drs397509210
GWAS Ctlgrs397509210
Max Magnitude0
ClinVar
Risk rs397509210(C;C)
Alt rs397509210(C;C)
Reference Rs397509210(T;T)
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.41222943A>G
CLNSRC ClinVar
CLNACC RCV000048720.2, RCV000258321.1,