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rs121918399

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918399(C;T)
Make rs121918399(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position44907843
GeneAPOE
is asnp
is mentioned by
dbSNPrs121918399
ebirs121918399
HLIrs121918399
Exacrs121918399
Varsomers121918399
Maprs121918399
PheGenIrs121918399
hapmaprs121918399
1000 genomesrs121918399
hgdprs121918399
ensemblrs121918399
gopubmedrs121918399
geneviewrs121918399
scholarrs121918399
googlers121918399
pharmgkbrs121918399
gwascentralrs121918399
openSNPrs121918399
23andMers121918399
23andMe allrs121918399
SNP Nexus

SNPshotrs121918399
SNPdbers121918399
MSV3drs121918399
GWAS Ctlgrs121918399
Max Magnitude0
OMIM107741
Desc
Variant0033
Relatedalso
ClinVar
Risk rs121918399(T;T)
Alt rs121918399(T;T)
Reference rs121918399(C;C)
Significance Pathogenic
Disease Lipoprotein glomerulopathy APOE KYOTO
Variation info
Gene APOE
CLNDBN Lipoprotein glomerulopathy APOE KYOTO
Reversed 0
HGVS NC_000019.9:g.45411100C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019468.27, RCV000019469.23,