rs6496589

Orientation

plus

Stabilized

plus

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

Make rs6496589(C;C)

Make rs6496589(C;G)

Reference

GRCh38 38.1/142

Chromosome

15

Position

89669998

Gene

PLIN1

is a	snp
is	mentioned by
dbSNP	rs6496589
dbSNP (classic)	rs6496589
ClinGen	rs6496589
ebi	rs6496589
HLI	rs6496589
Exac	rs6496589
Gnomad	rs6496589
Varsome	rs6496589
LitVar	rs6496589
Map	rs6496589
PheGenI	rs6496589
Biobank	rs6496589
1000 genomes	rs6496589
hgdp	rs6496589
ensembl	rs6496589
geneview	rs6496589
scholar	rs6496589
google	rs6496589
pharmgkb	rs6496589
gwascentral	rs6496589
openSNP	rs6496589
23andMe	rs6496589
SNPshot	rs6496589
SNPdbe	rs6496589
MSV3d	rs6496589
GWAS Ctlg	rs6496589

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 25529448] A functional variant in the exon 5 of PLIN1 reduces risk of central obesity by possible regulation of lipid storage

ClinVar
Risk	rs6496589(C;C) rs6496589(T;T)
Alt	rs6496589(C;C) rs6496589(T;T)
Reference	Rs6496589(G;G)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	PLIN1
CLNDBN	not specified
Reversed	0
HGVS	NC_000015.9:g.90213229G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000117994.2,