Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1033810883
rs1033810883
Entrez Id: 7471;7480
Gene Symbol: WNT1;WNT10B
WNT1;WNT10B
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.010 GeneticVariation BEFREE We also found a missense variant in WNT1 (S88R) that was overrepresented in the ASD sample (8 A/T in 267 ASD (minor allele frequency (MAF)=1.69%) vs 1 A/T in 377 controls (MAF=0.13%), OR=13.0, Fisher's exact test, P=0.0048; OR=8.2 and P=0.053 after correction for population stratification). 24002087 2013