Promoter region SNP position SNP ID Gene Disease Type P-value Source
chr12:389223-498486 chr12:421394 rs11062357 KDM5A Tourette syndrome intron 0.000202 GWASdb
chr12:389223-498486 chr12:427575 rs11062385 KDM5A Amyotrophic Lateral Sclerosis missense 0.000368 GWASdb
chr12:389223-498486 chr12:493900 rs1860360 KDM5A Amyotrophic Lateral Sclerosis intron 0.000945 GWASdb
chr12:389223-498486 chr12:442384 rs1048466 CCDC77 Obesity (early onset extreme) 3_prime_UTR_variant 8e-08 GWAS_Catalog
chr12:389223-498486 chr12:467818 rs11612228 B4GALNT3 Height intron_variant 7e-10 GWAS_Catalog