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SNP information rs11191580

RS11191580

Normal allele: CC

Polymorphism rs11191580 is related to topics like this:

DNA test for autism

We recommend that anyone who has been diagnosed with autism undergo genetic testing. Unfortunately,...

Schizophrenia is it genetic

A psychosis known as schizophrenia impacts an individual's thinking, sense of self, and...

Research and publications:

  20014157   Genetic association between intronic variants in AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10.

  21926974   Genome-wide association study identifies five new schizophrenia loci.

  22520855   Association study of a new schizophrenia susceptibility locus of 10q24.32-33 in a Han Chinese population.

  23507081   Using genetic, cognitive and multi-modal neuroimaging data to identify ultra-high-risk and first-episode psychosis at the individual level.

  23637625   Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate.

  23871474   A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation.

  24174267   A population-based study of genetic variation and psychotic experiences in adolescents.

  24339136   Neurophysiologic effect of GWAS derived schizophrenia and bipolar risk variants.

  24861553   Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index.

  27004590   Genome-wide significant schizophrenia risk variation on chromosome 10q24 is associated with altered cis-regulation of BORCS7, AS3MT, and NT5C2 in the human brain.

  27028512   Genetic Evaluation of Schizophrenia Using the Illumina HumanExome Chip.

  27759212   Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort.

  27895608   Genetic Consideration of Schizotypal Traits: A Review.

  28209224   Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

  28277567   Evidence of AS3MT(d2d3)-Associated Variants within 10q24.32-33 in the Genetic Risk of Major Affective Disorders.

  30610940   Replication of previous GWAS hits suggests the association between rs4307059 near MSNP1AS and autism in a Chinese Han population.

  32590138   Association between NT5C2 rs11191580 and autism spectrum disorder in the Chinese Han population.

  34247200   Associations between KCNQ1 and ITIH4 gene polymorphisms and infant weight gain in early life.

  35124268   Mendelian Randomization Analysis Reveals No Causal Relationship Between Nonalcoholic Fatty Liver Disease and Severe COVID-19.

Gene for lactose intolerance

Lactose intolerance is a condition characterized by difficulty digesting lactose, a sugar present...

CCNB1 cyclin B1

Cyclin B1 serves as a regulatory protein pivotal in the process of mitosis. It forms complexes with...

DNA methylation genes

The Genetic Methylation Check examines your DNA to offer insights into your unique methylation...

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