Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894761
rs104894761
AVPR2
0.810 GeneticVariation BEFREE We report on a family affected by NSIAD with the known mutation R137C, an arginine to cysteine substitution at amino acid 137. 22154540

2012
dbSNP: rs104894761
rs104894761
AVPR2
0.810 GeneticVariation UNIPROT Nephrogenic syndrome of inappropriate antidiuresis. 15872203

2005
dbSNP: rs104894761
rs104894761
AVPR2
T 0.810 CausalMutation CLINVAR