RS143797113 CLDN14

Health Risk Chr 21:36461208
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs143797113, also known as c.488C&gt
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 29
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 29
Monogenic hearing loss
Other Variants in CLDN14
rs786200885 rs74315437 rs74315438 rs139437157 rs149733854 rs387907417 rs577393948 rs727504989 rs368027306 rs371100799
Ask Dr. Hemsworth about this variant