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rs397509320

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509320(C;C)
Make rs397509320(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094742
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509320
ebirs397509320
HLIrs397509320
Exacrs397509320
Varsomers397509320
Maprs397509320
PheGenIrs397509320
hapmaprs397509320
1000 genomesrs397509320
hgdprs397509320
ensemblrs397509320
gopubmedrs397509320
geneviewrs397509320
scholarrs397509320
googlers397509320
pharmgkbrs397509320
gwascentralrs397509320
openSNPrs397509320
23andMers397509320
23andMe allrs397509320
SNP Nexus

SNPshotrs397509320
SNPdbers397509320
MSV3drs397509320
GWAS Ctlgrs397509320
Max Magnitude0
ClinVar
Risk rs397509320(C;C)
Alt rs397509320(C;C)
Reference rs397509320(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.41246759A>G
CLNSRC ClinVar
CLNACC RCV000049134.2,