RS267607135 TPRN

Health Risk Chr 9:137199473
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 79
Hearing loss
autosomal recessive
Autosomal recessive nonsyndromic hearing loss 79
Hearing loss
autosomal recessive
Other Variants in TPRN
rs387906219 rs387906220 rs387906221 rs387906222 rs727503520 rs140967677 rs139520402 rs377461469 rs548415902 rs559890679
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