Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777639(G;G)
Make rs587777639(G;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position143215033
GeneGPIHBP1
is asnp
is mentioned by
dbSNPrs587777639
ebirs587777639
HLIrs587777639
Exacrs587777639
Varsomers587777639
Maprs587777639
PheGenIrs587777639
hapmaprs587777639
1000 genomesrs587777639
hgdprs587777639
ensemblrs587777639
gopubmedrs587777639
geneviewrs587777639
scholarrs587777639
googlers587777639
pharmgkbrs587777639
gwascentralrs587777639
openSNPrs587777639
23andMers587777639
23andMe allrs587777639
SNP Nexus

SNPshotrs587777639
SNPdbers587777639
MSV3drs587777639
GWAS Ctlgrs587777639
Max Magnitude0
ClinVar
Risk rs587777639(G;G)
Alt rs587777639(G;G)
Reference rs587777639(T;T)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene GPIHBP1
CLNDBN Hyperlipoproteinemia, type ID
Reversed 0
HGVS NC_000008.10:g.144296908T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000133524.3,