CADM1, cell adhesion molecule 1, 23705

N. diseases: 205; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1048932
rs1048932
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1048932
rs1048932
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs6589488
rs6589488
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C0003125
Disease:
Anorexia Nervosa 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. 31308545 2019
dbSNP: rs4445669
rs4445669
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C0202230
Disease:
Thyroid stimulating hormone measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. 30367059 2018
dbSNP: rs1048932
rs1048932
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062 2017
dbSNP: rs528704957
rs528704957
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C1305855
Disease:
Body mass index 		G 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs5794958
rs5794958
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs11215400
rs11215400
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C1314691
Disease:
Age at menarche 		C 0.700 GeneticVariation GWASCAT Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. 25231870 2014
dbSNP: rs10891841
rs10891841
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10891841
rs10891841
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs17118345
rs17118345
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs10891819
rs10891819
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.010 GeneticVariation BEFREE <b>Results:</b> Nominal significant genotypic effect of rs10891819 in "ADHD-alone" subgroup was detected (<i>P</i> = 0.008) with TT genotype as protective. 31616473 2019
dbSNP: rs201292141
rs201292141
Entrez Id: 23705
Gene Symbol: CADM1
CADM1
CUI: C1510586
Disease:
Autism Spectrum Disorders 		0.010 GeneticVariation BEFREE We previously found two missense mutations, H246N and Y251S, in the gene-encoding synaptic cell adhesion molecule-1 (CADM1) in ASD patients, including cleavage of the mutated CADM1 and its intracellular accumulation. 21364653 2010