rs4743056
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4743056(C;C) |
Make rs4743056(C;T) |
Make rs4743056(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 97059329 |
is a | snp |
is | mentioned by |
dbSNP | rs4743056 |
dbSNP (classic) | rs4743056 |
ClinGen | rs4743056 |
ebi | rs4743056 |
HLI | rs4743056 |
Exac | rs4743056 |
Gnomad | rs4743056 |
Varsome | rs4743056 |
LitVar | rs4743056 |
Map | rs4743056 |
PheGenI | rs4743056 |
Biobank | rs4743056 |
1000 genomes | rs4743056 |
hgdp | rs4743056 |
ensembl | rs4743056 |
geneview | rs4743056 |
scholar | rs4743056 |
rs4743056 | |
pharmgkb | rs4743056 |
gwascentral | rs4743056 |
openSNP | rs4743056 |
23andMe | rs4743056 |
SNPshot | rs4743056 |
SNPdbe | rs4743056 |
MSV3d | rs4743056 |
GWAS Ctlg | rs4743056 |
GMAF | 0.494 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs4743056 increases susceptibility to Myasthenia gravis 1.37 times for carriers of the G allele [PMID 17869649]
rs4743056 increases susceptibility to Myasthenia gravis, early onset 1.61 times for carriers of the G allele [PMID 17869649]