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rs397509293

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509293(-;-)
Make rs397509293(-;G)
Make rs397509293(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045737
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509293
ebirs397509293
HLIrs397509293
Exacrs397509293
Varsomers397509293
Maprs397509293
PheGenIrs397509293
hapmaprs397509293
1000 genomesrs397509293
hgdprs397509293
ensemblrs397509293
gopubmedrs397509293
geneviewrs397509293
scholarrs397509293
googlers397509293
pharmgkbrs397509293
gwascentralrs397509293
openSNPrs397509293
23andMers397509293
23andMe allrs397509293
SNP Nexus

SNPshotrs397509293
SNPdbers397509293
MSV3drs397509293
GWAS Ctlgrs397509293
Max Magnitude0
ClinVar
Risk rs397509293(G;G)
Alt rs397509293(G;G)
Reference rs397509293(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41197754_41197755insC
CLNSRC ClinVar
CLNACC RCV000049039.2,