RS137853003 PCDH15

Health Risk Chr 10:54369194
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 23
Rare genetic deafness
Usher syndrome type 1F
Usher syndrome type 1F
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 23
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 23
Rare genetic deafness
Usher syndrome type 1F
Usher syndrome type 1F
Usher syndrome type 1
Autosomal recessive nonsyndromic hearing loss 23
Usher syndrome type 1
Other Variants in PCDH15
rs1307471318 rs137853001 rs199469706 rs111033260 rs137853002 rs137853004 rs267606932 rs201855435 rs483353074 rs141169746
Ask Dr. Hemsworth about this variant