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rs6496589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6496589(C;C)
Make rs6496589(C;G)
ReferenceGRCh38 38.1/142
Chromosome15
Position89669998
GenePLIN1
is asnp
is mentioned by
dbSNPrs6496589
ebirs6496589
HLIrs6496589
Exacrs6496589
Varsomers6496589
Maprs6496589
PheGenIrs6496589
hapmaprs6496589
1000 genomesrs6496589
hgdprs6496589
ensemblrs6496589
gopubmedrs6496589
geneviewrs6496589
scholarrs6496589
googlers6496589
pharmgkbrs6496589
gwascentralrs6496589
openSNPrs6496589
23andMers6496589
23andMe allrs6496589
SNP Nexus

SNPshotrs6496589
SNPdbers6496589
MSV3drs6496589
GWAS Ctlgrs6496589
Max Magnitude0
? (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)
Alt rs6496589(C;C)
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
CLNACC RCV000117994.2,