rs118204082

Orientation

plus

Stabilized

plus

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

Make rs118204082(C;G)

Make rs118204082(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

19955863

Gene

LPL

is a	snp
is	mentioned by
dbSNP	rs118204082
dbSNP (classic)	rs118204082
ClinGen	rs118204082
ebi	rs118204082
HLI	rs118204082
Exac	rs118204082
Gnomad	rs118204082
Varsome	rs118204082
LitVar	rs118204082
Map	rs118204082
PheGenI	rs118204082
Biobank	rs118204082
1000 genomes	rs118204082
hgdp	rs118204082
ensembl	rs118204082
geneview	rs118204082
scholar	rs118204082
google	rs118204082
pharmgkb	rs118204082
gwascentral	rs118204082
openSNP	rs118204082
23andMe	rs118204082
SNPshot	rs118204082
SNPdbe	rs118204082
MSV3d	rs118204082
GWAS Ctlg	rs118204082

Max Magnitude

0

OMIM	609708
Desc
Variant	0040
Related	also

ClinVar
Risk	rs118204082(G;G) rs118204082(T;T)
Alt	rs118204082(G;G) rs118204082(T;T)
Reference	Rs118204082(C;C)
Significance	Pathogenic
Disease	Hyperlipoproteinemia
Variation	info
Gene	LPL
CLNDBN	Hyperlipoproteinemia, type I
Reversed	0
HGVS	NC_000008.10:g.19813374C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001623.2,