COL13A1, collagen type XIII alpha 1 chain, 1305

N. diseases: 139; N. variants: 8
Disease: MYASTHENIC SYNDROME, CONGENITAL, 19 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554943789
rs1554943789
Entrez Id: 1305
Gene Symbol: COL13A1
COL13A1
CUI: C4225235
Disease:
MYASTHENIC SYNDROME, CONGENITAL, 19 		C 0.700 GeneticVariation CLINVAR