Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569032751
rs1569032751
A 0.700 GeneticVariation CLINVAR Selective resistance to parathyroid hormone caused by a novel uncoupling mutation in the carboxyl terminus of G alpha(s). A cause of pseudohypoparathyroidism type Ib. 11029463

2001

dbSNP: rs1569032751
rs1569032751
A 0.700 GeneticVariation CLINVAR Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy. 8699958

1996