GPR68, G protein-coupled receptor 68, 8111

N. diseases: 48; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057517672
rs1057517672
Entrez Id: 8111
Gene Symbol: GPR68
GPR68
CUI: C4310665
Disease:
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6 		0.800 GeneticVariation UNIPROT
dbSNP: rs1057517672
rs1057517672
Entrez Id: 8111
Gene Symbol: GPR68
GPR68
CUI: C4310665
Disease:
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6 		G 0.800 CausalMutation CLINVAR
dbSNP: rs1057517671
rs1057517671
Entrez Id: 8111
Gene Symbol: GPR68
GPR68
CUI: C4310665
Disease:
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1555409827
rs1555409827
Entrez Id: 8111
Gene Symbol: GPR68
GPR68
CUI: C4310665
Disease:
AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6 		C 0.700 CausalMutation CLINVAR