RS773404494 PCDH15

Health Risk Chr 10:53938830
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Usher syndrome type 1F
Autosomal recessive nonsyndromic hearing loss 23
Usher syndrome type 1D
PCDH15-related disorder
Rare genetic deafness
Usher syndrome type 1F
Autosomal recessive nonsyndromic hearing loss 23
Usher syndrome type 1D
PCDH15-related disorder
Other Variants in PCDH15
rs1307471318 rs137853001 rs199469706 rs111033260 rs137853002 rs137853003 rs137853004 rs267606932 rs201855435 rs483353074
Ask Dr. Hemsworth about this variant