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rs190853081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs190853081(A;A)
Make rs190853081(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44909083
GeneAPOE
is asnp
is mentioned by
dbSNPrs190853081
ebirs190853081
HLIrs190853081
Exacrs190853081
Varsomers190853081
Maprs190853081
PheGenIrs190853081
hapmaprs190853081
1000 genomesrs190853081
hgdprs190853081
ensemblrs190853081
gopubmedrs190853081
geneviewrs190853081
scholarrs190853081
googlers190853081
pharmgkbrs190853081
gwascentralrs190853081
openSNPrs190853081
23andMers190853081
23andMe allrs190853081
SNP Nexus

SNPshotrs190853081
SNPdbers190853081
MSV3drs190853081
GWAS Ctlgrs190853081
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs190853081(A;A)
Alt rs190853081(A;A)
Reference rs190853081(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.45412340G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019435.29,