RS387906221 TPRN

Health Risk Chr 9:137200476
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 79
Rare genetic deafness
TPRN-related disorder
Ear malformation
Autosomal recessive nonsyndromic hearing loss 79
Rare genetic deafness
TPRN-related disorder
Ear malformation
Other Variants in TPRN
rs267607135 rs387906219 rs387906220 rs387906222 rs727503520 rs140967677 rs139520402 rs377461469 rs548415902 rs559890679
Ask Dr. Hemsworth about this variant