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rs587777643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777643(C;G)
Make rs587777643(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position143215283
GeneGPIHBP1
is asnp
is mentioned by
dbSNPrs587777643
ebirs587777643
HLIrs587777643
Exacrs587777643
Varsomers587777643
Maprs587777643
PheGenIrs587777643
hapmaprs587777643
1000 genomesrs587777643
hgdprs587777643
ensemblrs587777643
gopubmedrs587777643
geneviewrs587777643
scholarrs587777643
googlers587777643
pharmgkbrs587777643
gwascentralrs587777643
openSNPrs587777643
23andMers587777643
23andMe allrs587777643
SNP Nexus

SNPshotrs587777643
SNPdbers587777643
MSV3drs587777643
GWAS Ctlgrs587777643
Max Magnitude0
ClinVar
Risk rs587777643(G;G)
Alt rs587777643(G;G)
Reference rs587777643(C;C)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene GPIHBP1
CLNDBN Hyperlipoproteinemia, type ID
Reversed 0
HGVS NC_000008.10:g.144297158C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000133530.4,