RS111033434 CLRN1

Health Risk Chr 3:150972581 snv missense variant
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What This Variant Does
"CLNSIG=4
Associated Conditions
Rare genetic deafness
Usher syndrome type 3A
Retinitis pigmentosa 61
Rare genetic deafness
Usher syndrome type 3A
Retinitis pigmentosa 61
Population Frequencies
gnomAD ALL
0%
Other Variants in CLRN1
rs121908140 rs121908141 rs1085307049 rs121908142 rs111033267 rs1553776036 rs121908143 rs374390376 rs397517930 rs397517932
Ask Dr. Hemsworth about this variant