rs964112
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs964112(G;G) |
Make rs964112(G;T) |
Make rs964112(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 31657400 |
Gene | ELP4 |
is a | snp |
is | mentioned by |
dbSNP | rs964112 |
dbSNP (classic) | rs964112 |
ClinGen | rs964112 |
ebi | rs964112 |
HLI | rs964112 |
Exac | rs964112 |
Gnomad | rs964112 |
Varsome | rs964112 |
LitVar | rs964112 |
Map | rs964112 |
PheGenI | rs964112 |
Biobank | rs964112 |
1000 genomes | rs964112 |
hgdp | rs964112 |
ensembl | rs964112 |
geneview | rs964112 |
scholar | rs964112 |
rs964112 | |
pharmgkb | rs964112 |
gwascentral | rs964112 |
openSNP | rs964112 |
23andMe | rs964112 |
SNPshot | rs964112 |
SNPdbe | rs964112 |
MSV3d | rs964112 |
GWAS Ctlg | rs964112 |
GMAF | 0.3062 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
rs964112 is a SNP in the elongator protein complex 4 ELP4 gene.
- Associated with rolandic epilepsy, as part of a relatively tightly linked cluster of 3 SNPs (rs964112, rs11031434, and rs986527.10.1038/ejhg.2008.267
[PMID 19172991] Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).