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rs397509210

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509210(C;C)
Make rs397509210(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43070926
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509210
ebirs397509210
HLIrs397509210
Exacrs397509210
Varsomers397509210
Maprs397509210
PheGenIrs397509210
hapmaprs397509210
1000 genomesrs397509210
hgdprs397509210
ensemblrs397509210
gopubmedrs397509210
geneviewrs397509210
scholarrs397509210
googlers397509210
pharmgkbrs397509210
gwascentralrs397509210
openSNPrs397509210
23andMers397509210
23andMe allrs397509210
SNP Nexus

SNPshotrs397509210
SNPdbers397509210
MSV3drs397509210
GWAS Ctlgrs397509210
Max Magnitude0
ClinVar
Risk rs397509210(C;C)
Alt rs397509210(C;C)
Reference rs397509210(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41222943A>G
CLNSRC ClinVar
CLNACC RCV000048720.2,