rs587777638

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs587777638(C;C)

Make rs587777638(C;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

143215025

Gene

GPIHBP1

is a	snp
is	mentioned by
dbSNP	rs587777638
dbSNP (classic)	rs587777638
ClinGen	rs587777638
ebi	rs587777638
HLI	rs587777638
Exac	rs587777638
Gnomad	rs587777638
Varsome	rs587777638
LitVar	rs587777638
Map	rs587777638
PheGenI	rs587777638
Biobank	rs587777638
1000 genomes	rs587777638
hgdp	rs587777638
ensembl	rs587777638
geneview	rs587777638
scholar	rs587777638
google	rs587777638
pharmgkb	rs587777638
gwascentral	rs587777638
openSNP	rs587777638
23andMe	rs587777638
SNPshot	rs587777638
SNPdbe	rs587777638
MSV3d	rs587777638
GWAS Ctlg	rs587777638

Max Magnitude

0

ClinVar
Risk	rs587777638(A;A) rs587777638(C;C)
Alt	rs587777638(A;A) rs587777638(C;C)
Reference	Rs587777638(G;G)
Significance	Pathogenic
Disease	Hyperlipoproteinemia
Variation	info
Gene	GPIHBP1
CLNDBN	Hyperlipoproteinemia, type ID
Reversed	0
HGVS	NC_000008.10:g.144296900G>A; NC_000008.10:g.144296900G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000133529.2, RCV000133523.4,