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rs587777641

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777641(A;C)
Make rs587777641(C;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position143215294
GeneGPIHBP1
is asnp
is mentioned by
dbSNPrs587777641
ebirs587777641
HLIrs587777641
Exacrs587777641
Varsomers587777641
Maprs587777641
PheGenIrs587777641
hapmaprs587777641
1000 genomesrs587777641
hgdprs587777641
ensemblrs587777641
gopubmedrs587777641
geneviewrs587777641
scholarrs587777641
googlers587777641
pharmgkbrs587777641
gwascentralrs587777641
openSNPrs587777641
23andMers587777641
23andMe allrs587777641
SNP Nexus

SNPshotrs587777641
SNPdbers587777641
MSV3drs587777641
GWAS Ctlgrs587777641
Max Magnitude0
ClinVar
Risk rs587777641(C;C)
Alt rs587777641(C;C)
Reference rs587777641(A;A)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene GPIHBP1
CLNDBN Hyperlipoproteinemia, type ID
Reversed 0
HGVS NC_000008.10:g.144297169A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133527.2,