Variant: rs869312749

present in Gene: DNMT1;S1PR2 present in Chromosome: 19 Position on Chromosome: 10224583 Alleles of this Variant: C/G

rs869312749 in DNMT1;S1PR2 gene and DEAFNESS, AUTOSOMAL RECESSIVE 68 PMID 26805784 2016 Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2.