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rs267606661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606661(C;G)
Make rs267606661(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44909101
GeneAPOE
is asnp
is mentioned by
dbSNPrs267606661
ebirs267606661
HLIrs267606661
Exacrs267606661
Varsomers267606661
Maprs267606661
PheGenIrs267606661
hapmaprs267606661
1000 genomesrs267606661
hgdprs267606661
ensemblrs267606661
gopubmedrs267606661
geneviewrs267606661
scholarrs267606661
googlers267606661
pharmgkbrs267606661
gwascentralrs267606661
openSNPrs267606661
23andMers267606661
23andMe allrs267606661
SNP Nexus

SNPshotrs267606661
SNPdbers267606661
MSV3drs267606661
GWAS Ctlgrs267606661
Max Magnitude0
ClinVar
Risk rs267606661(G,T;G,T)
Alt rs267606661(G,T;G,T)
Reference rs267606661(C;C)
Significance Pathogenic
Disease Familial type 3 hyperlipoproteinemia
Variation info
Gene APOE
CLNDBN Familial type 3 hyperlipoproteinemia
Reversed 0
HGVS NC_000019.9:g.45412358C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019455.28,