RS121908141 CLRN1

Health Risk Chr 3:150941655 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Usher syndrome type 3
Usher syndrome type 3
Population Frequencies
gnomAD ALL
100%
Other Variants in CLRN1
rs121908140 rs1085307049 rs121908142 rs111033267 rs1553776036 rs121908143 rs374390376 rs111033434 rs397517930 rs397517932
Ask Dr. Hemsworth about this variant