Table 1 Association of WNT1 rs61758378 with ASD
From: A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation
Sequenom genotyping | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Illumina sequencing | Confirmation sample set | Replication sample set | Combined sample set | P-value (combined samples) | |||||||
Gene | Reference | Function | ASD | Con | ASD | Con | ASD | Con | ASD | Con | |
WNT1 | rs61758378 | S88R | 0 AA | 0 AA | 0 AA | 0 AA | 0 AA | 0 AA | 0 AA | 0 AA | 0.0048 |
6 AT | 1 AT | 6 AT | 1 AT | 2 AT | 0 AT | 8 AT | 1 AT | ||||
192 TT | 239 TT | 189 TT | 238 TT | 70 TT | 138 TT | 259 TT | 376 TT |