Table 2 Genetic association analysis of CX3CR1-Ala55Thr

From: Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders

Exon

Ref

Val

Position

Variant

Case (SCZ+ASD)

Control

     

Allele count a

MAF

Odds ratio

P-valueb

Allele count a

MAF

2

G

A

3:39266347

p.Ala55Thr

7/6454

0.0011

8.3 (1.33–inf)

0.020

1/7652

0.00013

  1. Abbreviations: ASD, autism spectrum disorders; MAF, minor allele frequency; Ref, reference; SCZ, schizophrenia; Val, variant.
  2. aMinor allele/major allele.
  3. bP values were calculated by one-tailed Fisher’s exact test.
  4. Note: Genomic position is based on NCBI builds GRCh38. Amino acid position is based on NCBI reference sequence NP_001328.1.
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