LACC1, laccase domain containing 1, 144811

N. diseases: 35; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3764147
rs3764147
Entrez Id: 144811
Gene Symbol: LACC1
LACC1
CUI: C0023343
Disease:
Leprosy
0.820 GeneticVariation BEFREE We also confirmed the association between missense variant rs3764147 (c.760A>G [p.Ile254Val]) in the GWAS hit LACC1 (formerly C13orf31) and leprosy (p = 6.11 × 10<sup>-18</sup>, OR = 1.605). 29706348 2018
dbSNP: rs3764147
rs3764147
Entrez Id: 144811
Gene Symbol: LACC1
LACC1
CUI: C0023343
Disease:
Leprosy
0.820 GeneticVariation BEFREE Single-nucleotide variations in C13orf31 (LACC1) that encode p.C284R and p.I254V in a protein of unknown function (called 'FAMIN' here) are associated with increased risk for systemic juvenile idiopathic arthritis, leprosy and Crohn's disease. 27478939 2016
dbSNP: rs3764147
rs3764147
Entrez Id: 144811
Gene Symbol: LACC1
LACC1
CUI: C0023343
Disease:
Leprosy
0.820 GeneticVariation GWASDB Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy. 22019778 2011
dbSNP: rs3764147
rs3764147
Entrez Id: 144811
Gene Symbol: LACC1
LACC1
CUI: C0023343
Disease:
Leprosy
G 0.820 GeneticVariation GWASDB Genomewide association study of leprosy. 20018961 2009
dbSNP: rs3764147
rs3764147
Entrez Id: 144811
Gene Symbol: LACC1
LACC1
CUI: C0023343
Disease:
Leprosy
G 0.820 GeneticVariation GWASCAT Genomewide association study of leprosy. 20018961 2009