Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894326
rs104894326
AQP2 ; LOC101927318
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894328
rs104894328
AQP2 ; LOC101927318
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894329
rs104894329
AQP2 ; LOC101927318
C 0.700 CausalMutation CLINVAR

dbSNP: rs104894330
rs104894330
AQP2 ; LOC101927318
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894331
rs104894331
AQP2 ; LOC101927318
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894333
rs104894333
AQP2 ; LOC101927318
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894334
rs104894334
AQP2 ; LOC101927318
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894335
rs104894335
AQP2 ; LOC101927318
A 0.700 CausalMutation CLINVAR

dbSNP: rs104894336
rs104894336
AQP2
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894337
rs104894337
AQP2 ; LOC101927318
G 0.700 CausalMutation CLINVAR

dbSNP: rs104894338
rs104894338
AQP2 ; LOC101927318
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894339
rs104894339
AQP2 ; LOC101927318
T 0.700 CausalMutation CLINVAR

dbSNP: rs104894341
rs104894341
AQP2 ; LOC101927318
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565636541
rs1565636541
AQP2 ; LOC101927318
A 0.700 CausalMutation CLINVAR

dbSNP: rs28931580
rs28931580
AQP2
C 0.700 CausalMutation CLINVAR