HGF, hepatocyte growth factor, 3082

N. diseases: 671; N. variants: 22
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder) ×
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: rs137853235
rs137853235 		1.000 0.120 7 81752250 splice region variant C/T snv 4.0E-06
CUI: C1842342
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 39 (disorder) 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.700 0