rs11890028
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11890028(G;G) |
Make rs11890028(G;T) |
Make rs11890028(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 166086767 |
Gene | LOC101929680, SCN1A |
is a | snp |
is | mentioned by |
dbSNP | rs11890028 |
dbSNP (classic) | rs11890028 |
ClinGen | rs11890028 |
ebi | rs11890028 |
HLI | rs11890028 |
Exac | rs11890028 |
Gnomad | rs11890028 |
Varsome | rs11890028 |
LitVar | rs11890028 |
Map | rs11890028 |
PheGenI | rs11890028 |
Biobank | rs11890028 |
1000 genomes | rs11890028 |
hgdp | rs11890028 |
ensembl | rs11890028 |
geneview | rs11890028 |
scholar | rs11890028 |
rs11890028 | |
pharmgkb | rs11890028 |
gwascentral | rs11890028 |
openSNP | rs11890028 |
23andMe | rs11890028 |
SNPshot | rs11890028 |
SNPdbe | rs11890028 |
MSV3d | rs11890028 |
GWAS Ctlg | rs11890028 |
GMAF | 0.1974 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22949513] |
Trait | Epilepsy (generalized) |
Title | Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 |
Risk Allele | T |
P-val | 4E-6 |
Odds Ratio | 1.18 [1.09-1.27] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 2
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d