Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1557551678
rs1557551678
CLDN19
A 0.700 CausalMutation CLINVAR

dbSNP: rs1045642
rs1045642
ABCB1
0.010 GeneticVariation BEFREE Our results suggest that the MDR1 C3435T polymorphism may confer susceptibility to polydipsia in SCZ. 18543120

2008
dbSNP: rs2271933
rs2271933
HCRTR1
0.010 GeneticVariation BEFREE In any case, our results support the hypothesis that the HCRTR1 Ile408Val polymorphism may confer susceptibility to polydipsia in SCZ. 17999203

2007
dbSNP: rs1801028
rs1801028
DRD2
0.010 GeneticVariation BEFREE The three polymorphisms, -141C Ins/Del, Ser311Cys, and TaqIA, were genotyped in patients with polydipsia (n = 64) and in those without polydipsia (n = 91). 15850500

2005
dbSNP: rs755694590
rs755694590
AQP2 ; LOC101927318
0.010 GeneticVariation BEFREE Affected individuals with profound polyuria and polydipsia were homozygous for an autosomal recessive missense V168M mutation in the AQP2 gene. 15100362

2004