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rs2229707

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2229707(A;A)
Make rs2229707(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position74006202
GeneUCP3
is asnp
is mentioned by
dbSNPrs2229707
ebirs2229707
HLIrs2229707
Exacrs2229707
Varsomers2229707
Maprs2229707
PheGenIrs2229707
hapmaprs2229707
1000 genomesrs2229707
hgdprs2229707
ensemblrs2229707
gopubmedrs2229707
geneviewrs2229707
scholarrs2229707
googlers2229707
pharmgkbrs2229707
gwascentralrs2229707
openSNPrs2229707
23andMers2229707
23andMe allrs2229707
SNP Nexus

SNPshotrs2229707
SNPdbers2229707
MSV3drs2229707
GWAS Ctlgrs2229707
Merged fromRs2734830
GMAF0.03719
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM602044
Desc
Variant0001
Relatedalso


ClinVar
Risk rs2229707(A;A)
Alt rs2229707(A;A)
Reference rs2229707(G;G)
Significance Pathogenic
Disease UCP3 POLYMORPHISM G/A Obesity
Variation info
Gene UCP3
CLNDBN UCP3 POLYMORPHISM G/A Obesity, severe, and type II diabetes
Reversed 1
HGVS NC_000011.9:g.73717247C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008012.2, RCV000008013.3,



[PMID 17357083OA-icon.png] Medical sequencing at the extremes of human body mass.


GET Evidence
UCP3-V102I
aa_change Val102Ile
aa_change_short V102I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0413646
summary