Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13208776
rs13208776
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C0042900
Disease:
Vitiligo 		0.810 GeneticVariation BEFREE Our data shows that the variant rs13208776 in SMOC2 gene does not play a major role in increasing the risk of vitiligo in Jordanian Arab patients. 20965805 2011
dbSNP: rs13208776
rs13208776
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C0042900
Disease:
Vitiligo 		0.810 GeneticVariation GWASCAT Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8. 19890347 2010
dbSNP: rs13208776
rs13208776
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C0042900
Disease:
Vitiligo 		0.810 GeneticVariation GWASDB Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8. 19890347 2010
dbSNP: rs76307059
rs76307059
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C0424678
Disease:
Lean body mass 		0.700 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698 2019
dbSNP: rs76307059
rs76307059
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs786200927
rs786200927
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C3276551
Disease:
DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH 		T 0.700 CausalMutation CLINVAR
dbSNP: rs875989843
rs875989843
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C3276551
Disease:
DENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH 		A 0.700 CausalMutation CLINVAR
dbSNP: rs13208776
rs13208776
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C1847835
Disease:
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		0.010 GeneticVariation BEFREE Our data shows that the variant rs13208776 in SMOC2 gene does not play a major role in increasing the risk of vitiligo in Jordanian Arab patients. 20965805 2011
dbSNP: rs13208776
rs13208776
Entrez Id: 64094
Gene Symbol: SMOC2
SMOC2
CUI: C1304470
Disease:
Generalized vitiligo 		0.010 GeneticVariation BEFREE The region of association contains only one gene, SMOC2, within which SNP rs13208776 attained genome-wide significance for association with generalized vitiligo (P=8.51x10(-8)) at odds ratio 7.445 (95% confidence interval=3.56-15.53) for the high-risk allele and population attributable risk 28.00. 19890347 2010