rs4141463, MACROD2

N. diseases: 3
Disease: Autistic Disorder ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.820 GeneticVariation BEFREE Therefore, this family-based association study was performed in 640 Chinese Han autism trios to investigate the association between autism and 7 SNPs with genome-wide significance in previous GWAS (rs4307059 near MSNP1AS, rs4141463 in MACROD2, rs2535629 in ITIH3, rs11191454 in AS3MT, rs1625579 in MIR137HG, rs11191580 in NT5C2, and rs1409313 in CUEDC2). 30610940 2019
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.820 GeneticVariation BEFREE Therefore, this study does not provide support for the reported association between rs4141463 and autism. 21656903 2011
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.820 GeneticVariation GWASCAT A genome-wide scan for common alleles affecting risk for autism. 20663923 2010
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.820 GeneticVariation GWASDB A genome-wide scan for common alleles affecting risk for autism. 20663923 2010