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

rs267606663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606663(A;A)
Make rs267606663(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44909021
GeneAPOE
is asnp
is mentioned by
dbSNPrs267606663
ebirs267606663
HLIrs267606663
Exacrs267606663
Varsomers267606663
Maprs267606663
PheGenIrs267606663
hapmaprs267606663
1000 genomesrs267606663
hgdprs267606663
ensemblrs267606663
gopubmedrs267606663
geneviewrs267606663
scholarrs267606663
googlers267606663
pharmgkbrs267606663
gwascentralrs267606663
openSNPrs267606663
23andMers267606663
23andMe allrs267606663
SNP Nexus

SNPshotrs267606663
SNPdbers267606663
MSV3drs267606663
GWAS Ctlgrs267606663
Max Magnitude0
ClinVar
Risk rs267606663(A,C;A,C)
Alt rs267606663(A,C;A,C)
Reference rs267606663(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.45412278G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019452.28,