HMX1, H6 family homeobox 1, 3166

N. diseases: 23; N. variants: 1
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs876657398
rs876657398 		1.000 0.080 4 8868090 missense variant T/G snv
CUI: C2677500
Disease: Oculoauricular Syndrome
Oculoauricular Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0