rs7665090, MANBA

N. diseases: 6
Disease: CREST Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
CREST Syndrome
CUI: C0206138
Disease: CREST Syndrome
0.010 GeneticVariation BEFREE Furthermore, phenotype stratification showed an association between rs1372072 and rs11117432 with the limited cutaneous subgroup (lcSSc) (P adj = 4.45 × 10(-4) and P adj = 0.001), whereas rs7665090 was associated with the diffuse cutaneous subtype (dcSSc) (P adj = 0.003). 25880423 2015