rs2600683
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2600683(C;C) |
Make rs2600683(C;G) |
Make rs2600683(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 174765747 |
Gene | CHRNA1 |
is a | snp |
is | mentioned by |
dbSNP | rs2600683 |
dbSNP (classic) | rs2600683 |
ClinGen | rs2600683 |
ebi | rs2600683 |
HLI | rs2600683 |
Exac | rs2600683 |
Gnomad | rs2600683 |
Varsome | rs2600683 |
LitVar | rs2600683 |
Map | rs2600683 |
PheGenI | rs2600683 |
Biobank | rs2600683 |
1000 genomes | rs2600683 |
hgdp | rs2600683 |
ensembl | rs2600683 |
geneview | rs2600683 |
scholar | rs2600683 |
rs2600683 | |
pharmgkb | rs2600683 |
gwascentral | rs2600683 |
openSNP | rs2600683 |
23andMe | rs2600683 |
SNPshot | rs2600683 |
SNPdbe | rs2600683 |
MSV3d | rs2600683 |
GWAS Ctlg | rs2600683 |
GMAF | 0.1593 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
Rs2600683 | |
---|---|
PubMed | [PMID 17687331] |
Affy Probeset | SNP_A-1876238 |
Affy Orientation | same |
On GW 5.0 | |
Alleles A/B | C/G |
Ancestral | C |
Population | Caucasian |
Allele | C |
Case Freq. | 0.21 |
Control Freq. | 0.11 |
Odds Ratio Het | |
Odds Ratio Hom | |
Odds Ratio All | 2.36 |
Disease | Myasthenia gravis, early onset (EOMG) |
rs2600683 increases susceptibility to Myasthenia gravis, early onset 2.36 times for carriers of the C allele [PMID 17687331]