MEOX1, mesenchyme homeobox 1, 4222

N. diseases: 55; N. variants: 3
Disease: Klippel Feil syndrome recessive type ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs713993044
rs713993044
Entrez Id: 4222
Gene Symbol: MEOX1
MEOX1
CUI: C1859209
Disease:
Klippel Feil syndrome recessive type 		A 0.700 CausalMutation CLINVAR