Mutations in PGRN gene associated with the risk of psoriasis in Pakistan: a case control study

BMC Medical Genomics

Table 2 Summary of variants of PGRN gene in psoriasis patients and controls

SNPs	Chromosome position	SNP property	MAF
rs25646	17: 44350262	Exon 5	0.08546
rs850713	17: 44350364	Intron 5	0.2537
805 A/G	17: 44350897	Intron 7	–

Genomic DNA from psoriasis patients was used to amplify the 978 bp DNA fragment covering the targeted region of GRN gene. DNA sequencing was performed, and two PGRN SNP sites and one point mutation were identified

ISSN: 1755-8794