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rs587777640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777640(G;T)
Make rs587777640(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position143215097
GeneGPIHBP1
is asnp
is mentioned by
dbSNPrs587777640
ebirs587777640
HLIrs587777640
Exacrs587777640
Varsomers587777640
Maprs587777640
PheGenIrs587777640
hapmaprs587777640
1000 genomesrs587777640
hgdprs587777640
ensemblrs587777640
gopubmedrs587777640
geneviewrs587777640
scholarrs587777640
googlers587777640
pharmgkbrs587777640
gwascentralrs587777640
openSNPrs587777640
23andMers587777640
23andMe allrs587777640
SNP Nexus

SNPshotrs587777640
SNPdbers587777640
MSV3drs587777640
GWAS Ctlgrs587777640
Max Magnitude0
ClinVar
Risk rs587777640(T;T)
Alt rs587777640(T;T)
Reference rs587777640(G;G)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene GPIHBP1
CLNDBN Hyperlipoproteinemia, type ID
Reversed 0
HGVS NC_000008.10:g.144296972G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000133526.4,