rs796053494, TSC2

N. diseases: 1
Disease: Keratoconus ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Keratoconus
CUI: C0022578
Disease: Keratoconus
0.010 GeneticVariation BEFREE Two heterozygous missense TSC1 variants g.132896322A>T (c.3408A>T, p.Asp1136Glu) and g.132896452G>A (c.3278G>A, p.Arg1093Gln) were identified in three patients with nonsyndromic KC. 29261847 2017