RS786200885 CLDN14

Health Risk Chr 21:36461298
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What This Variant Does
"rs786200885, also known as c.398delT and p.Met133Argfs, represents a variant in the CLDN14 gene on c...
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 29
Autosomal recessive nonsyndromic hearing loss 29
Other Variants in CLDN14
rs74315437 rs74315438 rs139437157 rs149733854 rs387907417 rs577393948 rs727504989 rs368027306 rs371100799 rs786204841
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