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rs1805192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1805192(C;G)
Make rs1805192(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position12379739
GenePPARG
is asnp
is mentioned by
dbSNPrs1805192
ebirs1805192
HLIrs1805192
Exacrs1805192
Varsomers1805192
Maprs1805192
PheGenIrs1805192
hapmaprs1805192
1000 genomesrs1805192
hgdprs1805192
ensemblrs1805192
gopubmedrs1805192
geneviewrs1805192
scholarrs1805192
googlers1805192
pharmgkbrs1805192
gwascentralrs1805192
openSNPrs1805192
23andMers1805192
23andMe allrs1805192
SNP Nexus

SNPshotrs1805192
SNPdbers1805192
MSV3drs1805192
GWAS Ctlgrs1805192
Max Magnitude0

[PMID 19573164] Association Study and Mutation Analysis of Adiponectin Shows Association of Variants in APM1 with Complex Obesity in Women

OMIM601487
Desc
Variant0002
Relatedalso


ClinVar
Risk rs1805192(G;G)
Alt rs1805192(G;G)
Reference rs1805192(C;C)
Significance Other
Disease Diabetes mellitus Obesity Body mass index Intimal medial thickness of internal carotid artery
Variation info
Gene PPARG
CLNDBN Diabetes mellitus, noninsulin-dependent, modifier of Obesity, modifier of Body mass index, modifier of Intimal medial thickness of internal carotid artery, modifier of
Reversed 0
HGVS NC_000003.11:g.12421238C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008604.3, RCV000008605.3, RCV000008606.4, RCV000008607.3,



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