Gene: S1PR2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9294
Gene Symbol: S1PR2
S1PR2 		0.020 GeneticVariation phenotype BEFREE Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2. 26805784 2016
Entrez Id: 9294
Gene Symbol: S1PR2
S1PR2 		0.020 Biomarker phenotype BEFREE DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2. 16703383 2006