Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894756
rs104894756
0.710 GeneticVariation BEFREE R137H mutations have been reported previously to cause nephrogenic diabetes insipidus. 16843086

2006

dbSNP: rs104894748
rs104894748
0.710 GeneticVariation BEFREE In addition to the functional significance of the conserved cysteine residues, we have also analyzed the defects of two mutant V2 receptors which cause X-linked nephrogenic diabetes insipidus (NDI) by the introduction of additional cysteine residues into the second extracellular loop (mutants G185C, R202C). 10648821

2000

dbSNP: rs104894748
rs104894748
T 0.710 CausalMutation CLINVAR

dbSNP: rs104894756
rs104894756
A 0.710 CausalMutation CLINVAR

dbSNP: rs104894328
rs104894328
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894747
rs104894747
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894749
rs104894749
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894750
rs104894750
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894751
rs104894751
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894752
rs104894752
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894753
rs104894753
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894754
rs104894754
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894755
rs104894755
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894757
rs104894757
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894758
rs104894758
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894759
rs104894759
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894760
rs104894760
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894761
rs104894761
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1569545523
rs1569545523
C 0.700 CausalMutation CLINVAR

dbSNP: rs193922112
rs193922112
C 0.700 GeneticVariation CLINVAR

dbSNP: rs193922113
rs193922113
C 0.700 GeneticVariation CLINVAR

dbSNP: rs193922114
rs193922114
C 0.700 GeneticVariation CLINVAR

dbSNP: rs193922115
rs193922115
A 0.700 GeneticVariation CLINVAR

dbSNP: rs193922116
rs193922116
A 0.700 GeneticVariation CLINVAR

dbSNP: rs193922117
rs193922117
T 0.700 GeneticVariation CLINVAR