RS786204841 CLDN14

Health Risk Chr 21:36461002
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What This Variant Does
"rs786204841, also known as c.694G&gt
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 29
Autosomal recessive nonsyndromic hearing loss 29
Other Variants in CLDN14
rs786200885 rs74315437 rs74315438 rs139437157 rs149733854 rs387907417 rs577393948 rs727504989 rs368027306 rs371100799
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