Variant: rs4954218

present in Gene: MAP3K19 present in Chromosome: 2 Position on Chromosome: 135045855 Alleles of this Variant: G/T

rs4954218 in MAP3K19 gene and Corneal Topography PMID 21979947 2012 A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.

rs4954218 in MAP3K19 gene and Keratoconus PMID 21979947 2012 These findings suggest SNP rs4954218, located near the RAB3GAP1 gene, previously reported to be associated with corneal malformation, is a potential susceptibility locus for keratoconus.

rs4954218 in MAP3K19 gene and Leukemia, Myelocytic, Acute PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.