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rs118204064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs118204064(A;G)
Make rs118204064(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position19954126
GeneLPL
is asnp
is mentioned by
dbSNPrs118204064
ebirs118204064
HLIrs118204064
Exacrs118204064
Varsomers118204064
Maprs118204064
PheGenIrs118204064
hapmaprs118204064
1000 genomesrs118204064
hgdprs118204064
ensemblrs118204064
gopubmedrs118204064
geneviewrs118204064
scholarrs118204064
googlers118204064
pharmgkbrs118204064
gwascentralrs118204064
openSNPrs118204064
23andMers118204064
23andMe allrs118204064
SNP Nexus

SNPshotrs118204064
SNPdbers118204064
MSV3drs118204064
GWAS Ctlgrs118204064
Max Magnitude0
OMIM609708
Desc
Variant0013
Relatedalso
ClinVar
Risk rs118204064(G;G)
Alt rs118204064(G;G)
Reference rs118204064(A;A)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene LPL
CLNDBN Hyperlipoproteinemia, type I
Reversed 0
HGVS NC_000008.10:g.19811637A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001597.2,