rs118204073

Orientation

plus

Stabilized

plus

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

Make rs118204073(A;C)

Make rs118204073(C;C)

Reference

GRCh38 38.1/141

Chromosome

8

Position

19951825

Gene

LPL

is a	snp
is	mentioned by
dbSNP	rs118204073
dbSNP (classic)	rs118204073
ClinGen	rs118204073
ebi	rs118204073
HLI	rs118204073
Exac	rs118204073
Gnomad	rs118204073
Varsome	rs118204073
LitVar	rs118204073
Map	rs118204073
PheGenI	rs118204073
Biobank	rs118204073
1000 genomes	rs118204073
hgdp	rs118204073
ensembl	rs118204073
geneview	rs118204073
scholar	rs118204073
google	rs118204073
pharmgkb	rs118204073
gwascentral	rs118204073
openSNP	rs118204073
23andMe	rs118204073
SNPshot	rs118204073
SNPdbe	rs118204073
MSV3d	rs118204073
GWAS Ctlg	rs118204073

Max Magnitude

0

OMIM	609708
Desc
Variant	0027
Related	also

ClinVar
Risk	rs118204073(C;C)
Alt	rs118204073(C;C)
Reference	Rs118204073(A;A)
Significance	Pathogenic
Disease	Hyperlipoproteinemia
Variation	info
Gene	LPL
CLNDBN	Hyperlipoproteinemia, type I
Reversed	0
HGVS	NC_000008.10:g.19809336A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000001610.2,