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rs118204066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118204066(A;A)
Make rs118204066(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position19960988
GeneLPL
is asnp
is mentioned by
dbSNPrs118204066
ebirs118204066
HLIrs118204066
Exacrs118204066
Varsomers118204066
Maprs118204066
PheGenIrs118204066
hapmaprs118204066
1000 genomesrs118204066
hgdprs118204066
ensemblrs118204066
gopubmedrs118204066
geneviewrs118204066
scholarrs118204066
googlers118204066
pharmgkbrs118204066
gwascentralrs118204066
openSNPrs118204066
23andMers118204066
23andMe allrs118204066
SNP Nexus

SNPshotrs118204066
SNPdbers118204066
MSV3drs118204066
GWAS Ctlgrs118204066
Max Magnitude0
OMIM609708
Desc
Variant0017
Relatedalso
ClinVar
Risk rs118204066(A;A)
Alt rs118204066(A;A)
Reference rs118204066(G;G)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene LPL
CLNDBN Hyperlipoproteinemia, type I
Reversed 0
HGVS NC_000008.10:g.19818499G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001601.2,