UCP2, uncoupling protein 2, 7351

N. diseases: 235; N. variants: 5
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs659366
rs659366
Entrez Id: 7351
Gene Symbol: UCP2
UCP2
CUI: C1845050
Disease:
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS 		0.010 GeneticVariation BEFREE Participants who carried the G allele at rs659366 were more likely to develop PDR. 25396419 2014