Gene: CASR ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28936684
rs28936684
CASR
0.810 GeneticVariation UNIPROT

dbSNP: rs200620134
rs200620134
CASR
0.800 GeneticVariation UNIPROT

dbSNP: rs1060502855
rs1060502855
CASR
0.710 GeneticVariation UNIPROT

dbSNP: rs1057518933
rs1057518933
CASR
0.700 GeneticVariation UNIPROT

dbSNP: rs1064794290
rs1064794290
CASR
0.700 GeneticVariation UNIPROT

dbSNP: rs1064794291
rs1064794291
CASR
0.700 GeneticVariation UNIPROT

dbSNP: rs193922423
rs193922423
CASR
0.700 GeneticVariation UNIPROT

dbSNP: rs193922441
rs193922441
CASR
0.700 GeneticVariation UNIPROT

dbSNP: rs773146939
rs773146939
CASR
0.700 GeneticVariation UNIPROT

dbSNP: rs104893689
rs104893689
CASR
0.810 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs121909262
rs121909262
CASR
0.810 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs104893690
rs104893690
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs104893717
rs104893717
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs104893719
rs104893719
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs121909258
rs121909258
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs121909259
rs121909259
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs121909263
rs121909263
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs121909264
rs121909264
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs121909265
rs121909265
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs121909266
rs121909266
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs121909268
rs121909268
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs201851934
rs201851934
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs397514728
rs397514728
CASR
0.800 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs104893716
rs104893716
CASR
0.700 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993
dbSNP: rs1276839362
rs1276839362
CASR
0.700 GeneticVariation UNIPROT Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. 7916660

1993