Variant: rs113993961

present in Gene: WRN present in Chromosome: 8 Position on Chromosome: 31141680 Alleles of this Variant: G/C

rs113993961 in WRN gene and Werner Syndrome PMID 9225981 1997 Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population.

PMID 8602509 1996 Positional cloning of the Werner's syndrome gene.

PMID 10347997 1999 Prevalence of Werner's syndrome heterozygotes in Japan.

PMID 10543396 1999 Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products.

PMID 16673358 2006 The spectrum of WRN mutations in Werner syndrome patients.