RS900334407 HGF

Health Risk Chr 7:81755189
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 39
Autosomal recessive nonsyndromic hearing loss 39
Other Variants in HGF
rs137853235 rs1788701297 rs148714837 rs145494248 rs141774517 rs147075806 rs145598174 rs367800414 rs140790665 rs769438908
Ask Dr. Hemsworth about this variant