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rs397509236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509236(-;-)
Make rs397509236(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063332
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509236
ebirs397509236
HLIrs397509236
Exacrs397509236
Varsomers397509236
Maprs397509236
PheGenIrs397509236
hapmaprs397509236
1000 genomesrs397509236
hgdprs397509236
ensemblrs397509236
gopubmedrs397509236
geneviewrs397509236
scholarrs397509236
googlers397509236
pharmgkbrs397509236
gwascentralrs397509236
openSNPrs397509236
23andMers397509236
23andMe allrs397509236
SNP Nexus

SNPshotrs397509236
SNPdbers397509236
MSV3drs397509236
GWAS Ctlgrs397509236
Max Magnitude0
ClinVar
Risk rs397509236(;)
Alt rs397509236(;)
Reference rs397509236(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.41215349delC
CLNSRC ClinVar
CLNACC RCV000048849.2,