Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80358240
rs80358240
MLC1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.020 GeneticVariation BEFREE Recently, a Leu309Met mutation in WKL1 (MLC1, KIAA0027), a gene mapped to chromosome 22q13.33, was reported to co-segregate with periodic catatonia, a clinical sub-type of schizophrenia, in seven members of an extended pedigree. 11986987

2002
dbSNP: rs80358240
rs80358240
MLC1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.020 GeneticVariation BEFREE In addition, initial reports suggested that a rare variant in exon 11 (L309M) is involved in the etiology of schizophrenia, but recent studies have brought forward compelling arguments that genetic variants of MLC1 are not associated with schizophrenia. 12477442

2002