rs936170
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs936170(C;C) |
Make rs936170(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 123703970 |
Gene | LOC105369194, MYLK |
is a | snp |
is | mentioned by |
dbSNP | rs936170 |
dbSNP (classic) | rs936170 |
ClinGen | rs936170 |
ebi | rs936170 |
HLI | rs936170 |
Exac | rs936170 |
Gnomad | rs936170 |
Varsome | rs936170 |
LitVar | rs936170 |
Map | rs936170 |
PheGenI | rs936170 |
Biobank | rs936170 |
1000 genomes | rs936170 |
hgdp | rs936170 |
ensembl | rs936170 |
geneview | rs936170 |
scholar | rs936170 |
rs936170 | |
pharmgkb | rs936170 |
gwascentral | rs936170 |
openSNP | rs936170 |
23andMe | rs936170 |
SNPshot | rs936170 |
SNPdbe | rs936170 |
MSV3d | rs936170 |
GWAS Ctlg | rs936170 |
GMAF | 0.2397 |
Max Magnitude | 0 |
[PMID 22015949] An intronic MYLK variant associated with inflammatory lung disease regulates promoter activity of the smooth muscle myosin light chain kinase isoform[PMID 17472811] Polymorphisms in the myosin light chain kinase gene that confer risk of severe sepsis are associated with a lower risk of asthma.