RS786204428 CLRN1

Health Risk Chr 3:150972557
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What This Variant Does
"CLNSIG=255
Associated Conditions
Usher syndrome type 3
Rare genetic deafness
Retinal dystrophy
Retinitis pigmentosa 61
Usher syndrome type 3A
Usher syndrome type 3
Rare genetic deafness
Retinal dystrophy
Retinitis pigmentosa 61
Usher syndrome type 3A
Other Variants in CLRN1
rs121908140 rs121908141 rs1085307049 rs121908142 rs111033267 rs1553776036 rs121908143 rs374390376 rs111033434 rs397517930
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