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: Bi et al., 2014

DOI: 10.1186/1742-2094-11-100

Study population description: Han Chinese; 713 CP, 753 healthy controls

Regional classification: East Asia

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

Variant Reported allele or genotype Condition Condition description Disease status Odds ratio P value
rs1554606 G allele CP None Susceptibility 2.500 0.00700000
rs2069845 A allele CP None Susceptibility 2.300 0.09000000
rs2069837 A allele CP Male Susceptibility 1.334 0.02700000
rs2069837 AA genotype CP Male Susceptibility None 0.04100000
rs2069837 A allele CP Male, Spastic Susceptibility None 0.02100000
rs2069837 AA genotype CP Male, Spastic Susceptibility None 0.02400000
rs1800796 C allele CP Male, Spastic Susceptibility None 0.02200000
rs1800796 CC genotype CP Periventricular leukomalacia Severity None 0.04200000
rs1800796 CC genotype CP Premature rupture of membrane Severity None 0.00180000
rs2066992 T allele CP Male, Spastic Susceptibility None 0.04000000
rs2066992 TT genotype CP Male, Spastic Susceptibility None 0.04100000
rs2066992 TT genotype CP Premature rupture of membrane Severity None 0.01500000
rs1800796 CC genotype CP Male, Spastic Susceptibility None 0.02700000
rs2069832 G allele CP None Susceptibility 2.700 0.02000000
rs2069833 T allele CP None Susceptibility 2.400 0.05000000