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rs118204057

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 4 Hyperlipoproteinemia, type I
(A;G) 2 Carrier for Hyperlipoproteinemia, type I
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome8
Position19954222
GeneLPL
is asnp
is mentioned by
dbSNPrs118204057
ebirs118204057
HLIrs118204057
Exacrs118204057
Varsomers118204057
Maprs118204057
PheGenIrs118204057
hapmaprs118204057
1000 genomesrs118204057
hgdprs118204057
ensemblrs118204057
gopubmedrs118204057
geneviewrs118204057
scholarrs118204057
googlers118204057
pharmgkbrs118204057
gwascentralrs118204057
openSNPrs118204057
23andMers118204057
23andMe allrs118204057
SNP Nexus

SNPshotrs118204057
SNPdbers118204057
MSV3drs118204057
GWAS Ctlgrs118204057
Max Magnitude4
OMIM609708
Desc
Variant0002
Relatedalso
ClinVar
Risk rs118204057(A;A)
Alt rs118204057(A;A)
Reference rs118204057(G;G)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene LPL
CLNDBN Hyperlipoproteinemia, type I
Reversed 0
HGVS NC_000008.10:g.19811733G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001586.3,