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rs267606662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606662(C;C)
Make rs267606662(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44908804
GeneAPOE
is asnp
is mentioned by
dbSNPrs267606662
ebirs267606662
HLIrs267606662
Exacrs267606662
Varsomers267606662
Maprs267606662
PheGenIrs267606662
hapmaprs267606662
1000 genomesrs267606662
hgdprs267606662
ensemblrs267606662
gopubmedrs267606662
geneviewrs267606662
scholarrs267606662
googlers267606662
pharmgkbrs267606662
gwascentralrs267606662
openSNPrs267606662
23andMers267606662
23andMe allrs267606662
SNP Nexus

SNPshotrs267606662
SNPdbers267606662
MSV3drs267606662
GWAS Ctlgrs267606662
Max Magnitude0
ClinVar
Risk rs267606662(C;C)
Alt rs267606662(C;C)
Reference rs267606662(G;G)
Significance Pathogenic
Disease APOE3 VARIANT
Variation info
Gene APOE
CLNDBN APOE3 VARIANT
Reversed 0
HGVS NC_000019.9:g.45412061G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019459.28,