PRRX1, paired related homeobox 1, 5396

N. diseases: 134; N. variants: 11
Disease: Otocephaly ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122375
rs398122375
Entrez Id: 5396
Gene Symbol: PRRX1
PRRX1
CUI: C0265242
Disease:
Otocephaly 		G 0.700 CausalMutation CLINVAR
dbSNP: rs398122375
rs398122375
Entrez Id: 5396
Gene Symbol: PRRX1
PRRX1
CUI: C0265242
Disease:
Otocephaly 		GAAAA 0.700 CausalMutation CLINVAR