Variant: rs104893745 

    present in Gene: MITF
    present in Chromosome: 3
    Position on Chromosome: 69951882
    Alleles of this Variant: C/G

rs104893745 in MITF gene and Tietz syndrome PMID 10851256 2000 Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF.