RS397517452 PCDH15

Health Risk Chr 10:54079426
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What This Variant Does
"CLNSIG=5
Associated Conditions
Usher syndrome type 1F
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 23
Usher syndrome type 1F
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 23
Other Variants in PCDH15
rs1307471318 rs137853001 rs199469706 rs111033260 rs137853002 rs137853003 rs137853004 rs267606932 rs201855435 rs483353074
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