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rs936170

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs936170(C;C)
Make rs936170(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position123703970
GeneMYLK
is asnp
is mentioned by
dbSNPrs936170
ebirs936170
HLIrs936170
Exacrs936170
Varsomers936170
Maprs936170
PheGenIrs936170
hapmaprs936170
1000 genomesrs936170
hgdprs936170
ensemblrs936170
gopubmedrs936170
geneviewrs936170
scholarrs936170
googlers936170
pharmgkbrs936170
gwascentralrs936170
openSNPrs936170
23andMers936170
23andMe allrs936170
SNP Nexus

SNPshotrs936170
SNPdbers936170
MSV3drs936170
GWAS Ctlgrs936170
GMAF0.2397
Max Magnitude0

[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.