Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509287

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509287(C;C)
Make rs397509287(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43047638
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509287
ebirs397509287
HLIrs397509287
Exacrs397509287
Varsomers397509287
Maprs397509287
PheGenIrs397509287
hapmaprs397509287
1000 genomesrs397509287
hgdprs397509287
ensemblrs397509287
gopubmedrs397509287
geneviewrs397509287
scholarrs397509287
googlers397509287
pharmgkbrs397509287
gwascentralrs397509287
openSNPrs397509287
23andMers397509287
23andMe allrs397509287
SNP Nexus

SNPshotrs397509287
SNPdbers397509287
MSV3drs397509287
GWAS Ctlgrs397509287
Max Magnitude0
ClinVar
Risk rs397509287(C;C)
Alt rs397509287(C;C)
Reference rs397509287(G;G)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41199655C>G
CLNSRC ClinVar
CLNACC RCV000049004.2,