rs16969968, CHRNA5

N. diseases: 37
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.030 GeneticVariation BEFREE Our results show that rs16969968 on CHRNA5 is tightly linked to genetic susceptibility, psychotic symptoms and cognitive deficits in SCZ in an early-onset Chinese population, suggesting that CHRNA5 may play an important role in the etiology of SCZ. 30366711 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.030 GeneticVariation BEFREE One cis-eQTL, rs16969968, results in a functionally disruptive missense mutation in CHRNA5, a schizophrenia-implicated gene. 30142156 2018
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
0.030 GeneticVariation BEFREE The Asp398Asn risk allele is significantly associated with smoking severity independently in schizophrenia patient smokers (P = 0.001) and control smokers (P = 0.029). 21418140 2011