Have questions? Visit https://www.reddit.com/r/SNPedia

rs33928909

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs33928909(A;A)
Make rs33928909(A;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position25890771
GeneMYO18B
is asnp
is mentioned by
dbSNPrs33928909
ebirs33928909
HLIrs33928909
Exacrs33928909
Varsomers33928909
Maprs33928909
PheGenIrs33928909
hapmaprs33928909
1000 genomesrs33928909
hgdprs33928909
ensemblrs33928909
gopubmedrs33928909
geneviewrs33928909
scholarrs33928909
googlers33928909
pharmgkbrs33928909
gwascentralrs33928909
openSNPrs33928909
23andMers33928909
23andMe allrs33928909
SNP Nexus

SNPshotrs33928909
SNPdbers33928909
MSV3drs33928909
GWAS Ctlgrs33928909
GMAF0.0326
Max Magnitude0
Venter snp
Source plos
Gene MYO18B
allele A
frequency
sift TOLERATED
HuRef 1103691019590
Disease Association Defects in MYO18B are associated with lung cancer. Inactivated in half of the primary lung cancers and cell lines; the causes include deletions, mutations and promoter methylation.



GET Evidence
MYO18B-S1444T
aa_change Ser1444Thr
aa_change_short S1444T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.034296
summary