rs13208776, SMOC2

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Vitiligo
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
Vitiligo
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
Vitiligo
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
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
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
Generalized vitiligo
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