Study Findings

The Study Findings table contains information on the genetic findings of a particular NESHIE or CP genetic study. Variants with statistically-significant associations with NESHIE or CP have p-values < 0.05. Odds ratio values quantify the strength of association of a variant allele with NESHIE or CP.

Paper: Xia et al., 2018

DOI: 10.3389%2Ffneur.2018.00182

Study population description: Han Chinese; A total of 282 CP patients and 197 healthy controls

Regional classification: East Asia

Sequencing or genotyping methods: Genotyping using MassARRAY single nucleotide polymorphism platform

Variant Reported allele or genotype Condition Condition description Disease status Odds ratio P value
rs1800896 CC genotype CP Spastic tetraplegia Susceptibility None 0.03000000
rs3024490 T allele CP Spastic tetraplegia Susceptibility 0.573 0.00600000
rs3024490 T allele CP None Susceptibility 0.702 0.03300000
rs1800896 C allele CP None Susceptibility 0.696 0.03300000
rs1800871 G alelle CP Spastic tetraplegia Susceptibility 0.549 0.00300000
rs1554286 T allele CP Spastic tetraplegia Susceptibility 0.612 0.01500000
rs1518111 C allele CP Spastic tetraplegia Susceptibility 1.696 0.00900000
rs1800896 C allele CP Spastic tetraplegia Susceptibility 2.881 0.00600000
rs3024490 TT genotype CP Spastic tetraplegia Susceptibility None 0.02700000
rs1800871 GG genotype CP Spastic tetraplegia Susceptibility None 0.01200000
rs1554286 TT genotype CP Spastic tetraplegia Susceptibility None 0.03900000
rs1518111 CC genotype CP Spastic tetraplegia Susceptibility None 0.01800000