ARHGAP6, Rho GTPase activating protein 6, 395

N. diseases: 17; N. variants: 20
Disease: Amelogenesis Imperfecta ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894737
rs104894737
Entrez Id: 265;395
Gene Symbol: AMELX;ARHGAP6
AMELX;ARHGAP6
CUI: C0002452
Disease:
Amelogenesis Imperfecta 		0.010 GeneticVariation BEFREE Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta. 15111628 2004
dbSNP: rs104894738
rs104894738
Entrez Id: 265;395
Gene Symbol: AMELX;ARHGAP6
AMELX;ARHGAP6
CUI: C0002452
Disease:
Amelogenesis Imperfecta 		0.010 GeneticVariation BEFREE Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta. 15111628 2004