[PMID 22561193] Genotype patterns and characteristics of PRNP in the Korean population


[PMID 18347820] Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation.

rs2756271

Parent Gene: PRNP

Importance: 1
Less common allele: A = 43%
More common allele: G = 57%
My Genotype: Log In