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rs397509063

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509063(-;-)
Make rs397509063(-;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092118
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509063
ebirs397509063
HLIrs397509063
Exacrs397509063
Varsomers397509063
Maprs397509063
PheGenIrs397509063
hapmaprs397509063
1000 genomesrs397509063
hgdprs397509063
ensemblrs397509063
gopubmedrs397509063
geneviewrs397509063
scholarrs397509063
googlers397509063
pharmgkbrs397509063
gwascentralrs397509063
openSNPrs397509063
23andMers397509063
23andMe allrs397509063
SNP Nexus

SNPshotrs397509063
SNPdbers397509063
MSV3drs397509063
GWAS Ctlgrs397509063
Max Magnitude0
ClinVar
Risk rs397509063(;)
Alt rs397509063(;)
Reference rs397509063(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.41244135delC
CLNSRC ClinVar
CLNACC RCV000048183.2,