RS397517932 CLRN1
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What This Variant Does
"CLNSIG=255
Associated Conditions
Usher syndrome type 3
Rare genetic deafness
Usher syndrome
Usher syndrome type 3A
Retinitis pigmentosa 61
Usher syndrome type 3
Rare genetic deafness
Usher syndrome
Usher syndrome type 3A
Retinitis pigmentosa 61
Other Variants in CLRN1