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rs587777638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777638(C;C)
Make rs587777638(C;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position143215025
GeneGPIHBP1
is asnp
is mentioned by
dbSNPrs587777638
ebirs587777638
HLIrs587777638
Exacrs587777638
Varsomers587777638
Maprs587777638
PheGenIrs587777638
hapmaprs587777638
1000 genomesrs587777638
hgdprs587777638
ensemblrs587777638
gopubmedrs587777638
geneviewrs587777638
scholarrs587777638
googlers587777638
pharmgkbrs587777638
gwascentralrs587777638
openSNPrs587777638
23andMers587777638
23andMe allrs587777638
SNP Nexus

SNPshotrs587777638
SNPdbers587777638
MSV3drs587777638
GWAS Ctlgrs587777638
Max Magnitude0
ClinVar
Risk rs587777638(A,C;A,C)
Alt rs587777638(A,C;A,C)
Reference rs587777638(G;G)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene GPIHBP1
CLNDBN Hyperlipoproteinemia, type ID
Reversed 0
HGVS NC_000008.10:g.144296900G>A; NC_000008.10:g.144296900G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133529.2, RCV000133523.4,