RS111033267 CLRN1

Health Risk Chr 3:150972520
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What This Variant Does
"[OMIM:?]
Associated Conditions
Usher syndrome type 3
Retinitis pigmentosa
Rare genetic deafness
Usher syndrome type 3A
CLRN1-related disorder
Retinitis pigmentosa 61
Usher syndrome type 3
Retinitis pigmentosa
Rare genetic deafness
Usher syndrome type 3A
CLRN1-related disorder
Retinitis pigmentosa 61
Other Variants in CLRN1
rs121908140 rs121908141 rs1085307049 rs121908142 rs1553776036 rs121908143 rs374390376 rs111033434 rs397517930 rs397517932
Ask Dr. Hemsworth about this variant