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rs104894319

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894319(C;T)
Make rs104894319(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position74005844
GeneUCP3
is asnp
is mentioned by
dbSNPrs104894319
ebirs104894319
HLIrs104894319
Exacrs104894319
Varsomers104894319
Maprs104894319
PheGenIrs104894319
hapmaprs104894319
1000 genomesrs104894319
hgdprs104894319
ensemblrs104894319
gopubmedrs104894319
geneviewrs104894319
scholarrs104894319
googlers104894319
pharmgkbrs104894319
gwascentralrs104894319
openSNPrs104894319
23andMers104894319
23andMe allrs104894319
SNP Nexus

SNPshotrs104894319
SNPdbers104894319
MSV3drs104894319
GWAS Ctlgrs104894319
GMAF0.002755
Max Magnitude0
OMIM602044
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894319(T;T)
Alt rs104894319(T;T)
Reference rs104894319(C;C)
Significance Pathogenic
Disease Obesity
Variation info
Gene UCP3
CLNDBN Obesity, severe, and type II diabetes
Reversed 1
HGVS NC_000011.9:g.73716889G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008014.2,