RS397517451 PCDH15

Health Risk Chr 10:54664247
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What This Variant Does
"CLNSIG=5
Associated Conditions
USHER SYNDROME
TYPE ID/F
DIGENIC
Usher syndrome type 1F
Usher syndrome type 1
Rare genetic deafness
USHER SYNDROME
TYPE ID/F
DIGENIC
Usher syndrome type 1F
Usher syndrome type 1
Rare genetic deafness
Other Variants in PCDH15
rs1307471318 rs137853001 rs199469706 rs111033260 rs137853002 rs137853003 rs137853004 rs267606932 rs201855435 rs483353074
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