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rs140808909

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs140808909(A;A)
Make rs140808909(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44909080
GeneAPOE
is asnp
is mentioned by
dbSNPrs140808909
ebirs140808909
HLIrs140808909
Exacrs140808909
Varsomers140808909
Maprs140808909
PheGenIrs140808909
hapmaprs140808909
1000 genomesrs140808909
hgdprs140808909
ensemblrs140808909
gopubmedrs140808909
geneviewrs140808909
scholarrs140808909
googlers140808909
pharmgkbrs140808909
gwascentralrs140808909
openSNPrs140808909
23andMers140808909
23andMe allrs140808909
SNP Nexus

SNPshotrs140808909
SNPdbers140808909
MSV3drs140808909
GWAS Ctlgrs140808909
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs140808909(A;A)
Alt rs140808909(A;A)
Reference rs140808909(G;G)
Significance Pathogenic
Disease Familial type 3 hyperlipoproteinemia
Variation info
Gene APOE
CLNDBN Familial type 3 hyperlipoproteinemia
Reversed 0
HGVS NC_000019.9:g.45412337G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019435.29,