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rs17848368

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0
Make rs17848368(C;T)
Make rs17848368(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position74006298
GeneUCP3
is asnp
is mentioned by
dbSNPrs17848368
ebirs17848368
HLIrs17848368
Exacrs17848368
Varsomers17848368
Maprs17848368
PheGenIrs17848368
hapmaprs17848368
1000 genomesrs17848368
hgdprs17848368
ensemblrs17848368
gopubmedrs17848368
geneviewrs17848368
scholarrs17848368
googlers17848368
pharmgkbrs17848368
gwascentralrs17848368
openSNPrs17848368
23andMers17848368
23andMe allrs17848368
SNP Nexus

SNPshotrs17848368
SNPdbers17848368
MSV3drs17848368
GWAS Ctlgrs17848368
Max Magnitude0
OMIM602044
DescOBESITY, SEVERE, AND TYPE II DIABETES
Variant0004
Relatedalso
Neighborrs2734830
Distance97


ClinVar
Risk rs17848368(T;T)
Alt rs17848368(T;T)
Reference rs17848368(C;C)
Significance Pathogenic
Disease Obesity
Variation info
Gene UCP3
CLNDBN Obesity, severe, and type II diabetes
Reversed 1
HGVS NC_000011.9:g.73717343G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008017.1,