rs118204066

Orientation

plus

Stabilized

plus

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

Make rs118204066(A;A)

Make rs118204066(A;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

19960988

Gene

LPL

is a	snp
is	mentioned by
dbSNP	rs118204066
dbSNP (classic)	rs118204066
ClinGen	rs118204066
ebi	rs118204066
HLI	rs118204066
Exac	rs118204066
Gnomad	rs118204066
Varsome	rs118204066
LitVar	rs118204066
Map	rs118204066
PheGenI	rs118204066
Biobank	rs118204066
1000 genomes	rs118204066
hgdp	rs118204066
ensembl	rs118204066
geneview	rs118204066
scholar	rs118204066
google	rs118204066
pharmgkb	rs118204066
gwascentral	rs118204066
openSNP	rs118204066
23andMe	rs118204066
SNPshot	rs118204066
SNPdbe	rs118204066
MSV3d	rs118204066
GWAS Ctlg	rs118204066

Max Magnitude

0

OMIM	609708
Desc
Variant	0017
Related	also

ClinVar
Risk	rs118204066(A;A)
Alt	rs118204066(A;A)
Reference	Rs118204066(G;G)
Significance	Pathogenic
Disease	Hyperlipoproteinemia
Variation	info
Gene	LPL
CLNDBN	Hyperlipoproteinemia, type I
Reversed	0
HGVS	NC_000008.10:g.19818499G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000001601.2,