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rs397509296

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509296(-;-)
Make rs397509296(-;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045722
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509296
ebirs397509296
HLIrs397509296
Exacrs397509296
Varsomers397509296
Maprs397509296
PheGenIrs397509296
hapmaprs397509296
1000 genomesrs397509296
hgdprs397509296
ensemblrs397509296
gopubmedrs397509296
geneviewrs397509296
scholarrs397509296
googlers397509296
pharmgkbrs397509296
gwascentralrs397509296
openSNPrs397509296
23andMers397509296
23andMe allrs397509296
SNP Nexus

SNPshotrs397509296
SNPdbers397509296
MSV3drs397509296
GWAS Ctlgrs397509296
Max Magnitude0
ClinVar
Risk rs397509296(;)
Alt rs397509296(;)
Reference rs397509296(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.41197739delG
CLNSRC ClinVar
CLNACC RCV000049045.2,