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rs587777637

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777637(A;C)
Make rs587777637(C;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position143215307
GeneGPIHBP1
is asnp
is mentioned by
dbSNPrs587777637
ebirs587777637
HLIrs587777637
Exacrs587777637
Varsomers587777637
Maprs587777637
PheGenIrs587777637
hapmaprs587777637
1000 genomesrs587777637
hgdprs587777637
ensemblrs587777637
gopubmedrs587777637
geneviewrs587777637
scholarrs587777637
googlers587777637
pharmgkbrs587777637
gwascentralrs587777637
openSNPrs587777637
23andMers587777637
23andMe allrs587777637
SNP Nexus

SNPshotrs587777637
SNPdbers587777637
MSV3drs587777637
GWAS Ctlgrs587777637
Max Magnitude0
ClinVar
Risk rs587777637(C;C)
Alt rs587777637(C;C)
Reference rs587777637(A;A)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene GPIHBP1
CLNDBN Hyperlipoproteinemia, type ID
Reversed 0
HGVS NC_000008.10:g.144297182A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133522.4,