PRDX2, peroxiredoxin 2, 7001

N. diseases: 243; N. variants: 2
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1055679036
rs1055679036
1.000 0.120 19 12800207 missense variant A/G snv
Gerstmann-Straussler-Scheinker Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Infections; Nervous System Diseases 0.020 1.000 2 2018 2019
dbSNP: rs775414901
rs775414901
1.000 0.080 19 12801169 synonymous variant C/G;T snv 3.6E-05
Amyotrophic Lateral Sclerosis, Familial
Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2004 2004