Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.850 GeneticVariation BEFREE To answer this question, we examined the association of rs10503253 with schizophrenia</span> in a total of 751</span>4 schizo</span>phrenia patients, 9058 healthy controls and 1115 nuclear families originated from Asia using a meta-analytic approach. 28344127

2017
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.850 GeneticVariation BEFREE Our findings do not support an association between CSMD1 rs10503253 and SCZ in a Han Chinese population. 27377754

2016
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.850 GeneticVariation BEFREE We investigated the neurocognitive effects of the CSMD1 rs10503253 (C/A) polymorphism in a large, demographically homogeneous sample of young, healthy Greek Caucasian males (n=1149) phenotyped for a wide range of neuropsychological measures, most of which have been shown to be reliable endophenotypes for schizophrenia. 24630139

2014
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.850 GeneticVariation BEFREE Neural effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. 23839771

2013
dbSNP: rs10503253
rs10503253
CSMD1
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.850 GeneticVariation BEFREE Neuropsychological effects of the CSMD1 genome-wide associated schizophrenia risk variant rs10503253. 23320435

2013