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rs145844329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145844329(C;C)
Make rs145844329(C;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position143215486
GeneGPIHBP1
is asnp
is mentioned by
dbSNPrs145844329
ebirs145844329
HLIrs145844329
Exacrs145844329
Varsomers145844329
Maprs145844329
PheGenIrs145844329
hapmaprs145844329
1000 genomesrs145844329
hgdprs145844329
ensemblrs145844329
gopubmedrs145844329
geneviewrs145844329
scholarrs145844329
googlers145844329
pharmgkbrs145844329
gwascentralrs145844329
openSNPrs145844329
23andMers145844329
23andMe allrs145844329
SNP Nexus

SNPshotrs145844329
SNPdbers145844329
MSV3drs145844329
GWAS Ctlgrs145844329
Max Magnitude0
ClinVar
Risk rs145844329(A,C;A,C)
Alt rs145844329(A,C;A,C)
Reference rs145844329(G;G)
Significance Pathogenic
Disease Hyperlipoproteinemia
Variation info
Gene GPIHBP1
CLNDBN Hyperlipoproteinemia, type ID
Reversed 0
HGVS NC_000008.10:g.144297361G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000133525.3,