CNP variant
Evidence from:
primary |
all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| CNP | associated_with | body weight | — | 1 |
| CNP | associated_with | Crohn’s disease | — | 1 |
| CNP | associated_with | HapMap CEU | — | 2 |
| CNP | interacts_with | SNP | — | 1 |
| SNP | interacts_with | CNP | — | 1 |
Mentioned in (9)
Papers in which this entity is mentioned.
- The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
- Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization. (2011)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. (2010)
- DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing. (2010)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. (2009)
- Finding the missing heritability of complex diseases. (2009)
- Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. (2005)
Merged raw entities (7)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| cnp | variant | 6 | 8 |
| copy number polymorphism | variant | 3 | 3 |
| cnps | variant | 2 | 2 |
| common copy number polymorphism | variant | — | — |
| common copy number polymorphisms | variant | — | — |
| diallelic copy number polymorphism | variant | — | — |
| human copy number variation | variant | — | — |