RS780953179 TPRN

Health Risk Chr 9:137199618
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 79
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 79
Other Variants in TPRN
rs267607135 rs387906219 rs387906220 rs387906221 rs387906222 rs727503520 rs140967677 rs139520402 rs377461469 rs548415902
Ask Dr. Hemsworth about this variant