Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518907
rs1057518907
GNAS
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia 		T 0.700 CausalMutation CLINVAR

dbSNP: rs137854539
rs137854539
GNAS
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs587777011
rs587777011
FAM111A
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia 		A 0.700 CausalMutation CLINVAR