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rs397509338

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509338(C;T)
Make rs397509338(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094603
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509338
ebirs397509338
HLIrs397509338
Exacrs397509338
Varsomers397509338
Maprs397509338
PheGenIrs397509338
hapmaprs397509338
1000 genomesrs397509338
hgdprs397509338
ensemblrs397509338
gopubmedrs397509338
geneviewrs397509338
scholarrs397509338
googlers397509338
pharmgkbrs397509338
gwascentralrs397509338
openSNPrs397509338
23andMers397509338
23andMe allrs397509338
SNP Nexus

SNPshotrs397509338
SNPdbers397509338
MSV3drs397509338
GWAS Ctlgrs397509338
Max Magnitude0
ClinVar
Risk rs397509338(T;T)
Alt rs397509338(T;T)
Reference rs397509338(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41246620G>A
CLNSRC ClinVar
CLNACC RCV000049193.2,