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rs11083750

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs11083750(C;G)
Make rs11083750(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44908601
GeneAPOE
is asnp
is mentioned by
dbSNPrs11083750
ebirs11083750
HLIrs11083750
Exacrs11083750
Varsomers11083750
Maprs11083750
PheGenIrs11083750
hapmaprs11083750
1000 genomesrs11083750
hgdprs11083750
ensemblrs11083750
gopubmedrs11083750
geneviewrs11083750
scholarrs11083750
googlers11083750
pharmgkbrs11083750
gwascentralrs11083750
openSNPrs11083750
23andMers11083750
23andMe allrs11083750
SNP Nexus

SNPshotrs11083750
SNPdbers11083750
MSV3drs11083750
GWAS Ctlgrs11083750
Max Magnitude0
OMIM107741
DescAPOE4 VARIANT
Variant0025
Relatedalso
Neighborrs28931576
Distance707
Neighborrs28931577
Distance44
ClinVar
Risk rs11083750(A,G,T;A,G,T)
Alt rs11083750(A,G,T;A,G,T)
Reference rs11083750(C;C)
Significance Other
Disease APOE4 VARIANT
Variation info
Gene APOE
CLNDBN APOE4 VARIANT
Reversed 0
HGVS NC_000019.9:g.45411858C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019458.24,