RS111033258 CLRN1;CLRN1-AS1
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What This Variant Does
"rs111033258, also known as N48K or Asn48Lys, is a SNP in the clarin 1 CLRN1 gene on chromosome 3. Mo...
Associated Conditions
Usher syndrome type 3
Retinitis pigmentosa
Retinal dystrophy
Usher syndrome type 3A
Retinitis pigmentosa 61
Usher syndrome type 3
Retinitis pigmentosa
Retinal dystrophy
Usher syndrome type 3A
Retinitis pigmentosa 61
Other Variants in CLRN1;CLRN1-AS1