Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12197901
rs12197901
Entrez Id: 93663
Gene Symbol: ARHGAP18
ARHGAP18
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE In addition, the allelic frequencies of rs12197901 remained associated with SZ in the combined cohort (P = 0.021), although not in the validation cohort alone (P = 0.251). 28384650 2017
dbSNP: rs7758025
rs7758025
Entrez Id: 93663
Gene Symbol: ARHGAP18
ARHGAP18
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE The AG haplotype in rs7758025-rs9385502 was strongly associated with the occurrence of SZ (P = 0.0012, OR = 0.67, 95% CI = 0.48-0.93), an association that still held following a 1000-times random permutation test (P = 0.022). 28384650 2017
dbSNP: rs9385502
rs9385502
Entrez Id: 93663
Gene Symbol: ARHGAP18
ARHGAP18
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE The AG haplotype in rs7758025-rs9385502 was strongly associated with the occurrence of SZ (P = 0.0012, OR = 0.67, 95% CI = 0.48-0.93), an association that still held following a 1000-times random permutation test (P = 0.022). 28384650 2017
dbSNP: rs9483050
rs9483050
Entrez Id: 93663
Gene Symbol: ARHGAP18
ARHGAP18
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE In an independently collected validation cohort, rs9483050 was the SNP most strongly associated with SZ. 28384650 2017