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rs1009388

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
Make rs1009388(C;G)
Make rs1009388(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position25168232
GenePOMC
is asnp
is mentioned by
dbSNPrs1009388
ebirs1009388
HLIrs1009388
Exacrs1009388
Varsomers1009388
Maprs1009388
PheGenIrs1009388
hapmaprs1009388
1000 genomesrs1009388
hgdprs1009388
ensemblrs1009388
gopubmedrs1009388
geneviewrs1009388
scholarrs1009388
googlers1009388
pharmgkbrs1009388
gwascentralrs1009388
openSNPrs1009388
23andMers1009388
23andMe allrs1009388
SNP Nexus

SNPshotrs1009388
SNPdbers1009388
MSV3drs1009388
GWAS Ctlgrs1009388
GMAF0.1566
Max Magnitude0
OMIM605552
DescABDOMINAL OBESITY-METABOLIC SYNDROME
Variant
Relatedalso
OMIM176830
DescPROOPIOMELANOCORTIN; POMC
Variant
Relatedalso


[PMID 21723177] Association analysis of proopiomelanocortin (POMC) haplotypes in type 1 diabetes in a UK population

[PMID 19217079OA-icon.png] Pro-opiomelanocortin gene variation related to alcohol or drug dependence: evidence and replications across family- and population-based studies.

[PMID 19337797] Association between variants in the genes for leptin, leptin receptor, and proopiomelanocortin with chronic heart failure in the Czech population.