rs118204078

Orientation

plus

Stabilized

plus

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

Make rs118204078(C;G)

Make rs118204078(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

19960935

Gene

LPL

is a	snp
is	mentioned by
dbSNP	rs118204078
dbSNP (classic)	rs118204078
ClinGen	rs118204078
ebi	rs118204078
HLI	rs118204078
Exac	rs118204078
Gnomad	rs118204078
Varsome	rs118204078
LitVar	rs118204078
Map	rs118204078
PheGenI	rs118204078
Biobank	rs118204078
1000 genomes	rs118204078
hgdp	rs118204078
ensembl	rs118204078
geneview	rs118204078
scholar	rs118204078
google	rs118204078
pharmgkb	rs118204078
gwascentral	rs118204078
openSNP	rs118204078
23andMe	rs118204078
SNPshot	rs118204078
SNPdbe	rs118204078
MSV3d	rs118204078
GWAS Ctlg	rs118204078

Max Magnitude

0

OMIM	609708
Desc
Variant	0034
Related	also

ClinVar
Risk	rs118204078(G;G)
Alt	rs118204078(G;G)
Reference	Rs118204078(C;C)
Significance	Pathogenic
Disease	Hyperlipoproteinemia
Variation	info
Gene	LPL
CLNDBN	Hyperlipoproteinemia, type I
Reversed	0
HGVS	NC_000008.10:g.19818446C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001616.2,