Variant: rs1177198729 

    present in Gene: USH2A;LOC105372918
    present in Chromosome: 1
    Position on Chromosome: 216196630
    Alleles of this Variant: C/A;G

rs1177198729 in USH2A;LOC105372918 gene and RETINITIS PIGMENTOSA 39 (disorder) PMID 16963483 2007 Development of a genotyping microarray for Usher syndrome.

PMID 25525159 2015 RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.

rs1177198729 in USH2A;LOC105372918 gene and USHER SYNDROME, TYPE IIA PMID 25525159 2015 RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.

PMID 16963483 2007 Development of a genotyping microarray for Usher syndrome.