OPN4, opsin 4, 94233

N. diseases: 87; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12257301
rs12257301
Entrez Id: 94233
Gene Symbol: OPN4
OPN4
CUI: C1704436
Disease:
Peripheral Arterial Diseases
0.700 GeneticVariation GWASCAT Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease. 27082954 2016
dbSNP: rs2675703
rs2675703
Entrez Id: 94233
Gene Symbol: OPN4
OPN4
CUI: C0085159
Disease:
Seasonal Affective Disorder
0.020 GeneticVariation BEFREE Two single-nucleotide polymorphisms (SNPs) in human melanopsin (hOPN4), Pro10Leu and Thr394Ile, have recently been associated with abnormal NIF responses to light, including seasonal affective disorder. 29718372 2018
dbSNP: rs2675703
rs2675703
Entrez Id: 94233
Gene Symbol: OPN4
OPN4
CUI: C0085159
Disease:
Seasonal Affective Disorder
0.020 GeneticVariation BEFREE Individuals with the T/T genotype were 5.6 times more likely to be in the SAD group than the control group, and all 7 (5%) of individuals with the T/T genotype at P10L were in the SAD group. 18804284 2009
dbSNP: rs1079610
rs1079610
Entrez Id: 94233;105378409
Gene Symbol: OPN4;LOC105378409
OPN4;LOC105378409
CUI: C0085159
Disease:
Seasonal Affective Disorder
0.010 GeneticVariation BEFREE Two single-nucleotide polymorphisms (SNPs) in human melanopsin (hOPN4), Pro10Leu and Thr394Ile, have recently been associated with abnormal NIF responses to light, including seasonal affective disorder. 29718372 2018