rs4349633
| Orientation | plus |
| Stabilized | plus |
| Make rs4349633(A;A) |
| Make rs4349633(A;G) |
| Make rs4349633(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 41483195 |
| Gene | LIMCH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4349633 |
| dbSNP (classic) | rs4349633 |
| ClinGen | rs4349633 |
| ebi | rs4349633 |
| HLI | rs4349633 |
| Exac | rs4349633 |
| Gnomad | rs4349633 |
| Varsome | rs4349633 |
| LitVar | rs4349633 |
| Map | rs4349633 |
| PheGenI | rs4349633 |
| Biobank | rs4349633 |
| 1000 genomes | rs4349633 |
| hgdp | rs4349633 |
| ensembl | rs4349633 |
| geneview | rs4349633 |
| scholar | rs4349633 |
| rs4349633 | |
| pharmgkb | rs4349633 |
| gwascentral | rs4349633 |
| openSNP | rs4349633 |
| 23andMe | rs4349633 |
| SNPshot | rs4349633 |
| SNPdbe | rs4349633 |
| MSV3d | rs4349633 |
| GWAS Ctlg | rs4349633 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Region with strongest linkage for ability to discriminate pitch found in study of 767 Finnish individuals belonging in 76 families [PMID 24614497
], involved in musical aptitude. Posterior Probability of Linkage given as 86% to trait Carl Seashore's subtest of pitch (SP).
Located next to the region harboring the protocadherin 7 gene, PCDH7 which has been suggested to play a role in cochlear and amygdaloid complexes. This SNP is in LIMCH1 LIM and calponin homology domains 1 gene, which is thought to be unlikely to be responsible, probably a combination of SNP's frequently inherited with it are involved. The study suggests rs13146789 in PCDH7 as one likely causal variant.
Publications[edit]
[PMID 24614497
] A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions.
- Is a snp
- In dbSNP
- SNPs on chromosome 4
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
