rs886037775

Orientation

plus

Stabilized

plus

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

Make rs886037775(A;T)

Make rs886037775(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

8

Position

19960948

Gene

LPL

is a	snp
is	mentioned by
dbSNP	rs886037775
dbSNP (classic)	rs886037775
ClinGen	rs886037775
ebi	rs886037775
HLI	rs886037775
Exac	rs886037775
Gnomad	rs886037775
Varsome	rs886037775
LitVar	rs886037775
Map	rs886037775
PheGenI	rs886037775
Biobank	rs886037775
1000 genomes	rs886037775
hgdp	rs886037775
ensembl	rs886037775
geneview	rs886037775
scholar	rs886037775
google	rs886037775
pharmgkb	rs886037775
gwascentral	rs886037775
openSNP	rs886037775
23andMe	rs886037775
SNPshot	rs886037775
SNPdbe	rs886037775
MSV3d	rs886037775
GWAS Ctlg	rs886037775

Max Magnitude

0

ClinVar
Risk	rs886037775(T;T)
Alt	rs886037775(T;T)
Reference	Rs886037775(A;A)
Significance	Probable-Pathogenic
Disease	Hyperlipoproteinemia
Variation	info
Gene	LPL
CLNDBN	Hyperlipoproteinemia, type I
Reversed	0
HGVS	NC_000008.10:g.19818459A>T
CLNSRC
CLNACC	RCV000258507.1,