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rs133885

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 0
Make rs133885(A;A)
Make rs133885(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position25763322
GeneMYO18B
is asnp
is mentioned by
dbSNPrs133885
ebirs133885
HLIrs133885
Exacrs133885
Varsomers133885
Maprs133885
PheGenIrs133885
hapmaprs133885
1000 genomesrs133885
hgdprs133885
ensemblrs133885
gopubmedrs133885
geneviewrs133885
scholarrs133885
googlers133885
pharmgkbrs133885
gwascentralrs133885
openSNPrs133885
23andMers133885
23andMe allrs133885
SNP Nexus

SNPshotrs133885
SNPdbers133885
MSV3drs133885
GWAS Ctlgrs133885
GMAF0.3186
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene MYO18B
allele A
frequency 0.458
sift
HuRef 1103691019299
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-G44E
aa_change Gly44Glu
aa_change_short G44E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.575026
summary



GWAS snp
PMID [PMID 23423138OA-icon.png]
Trait Mathematical ability in children with dyslexia
Title A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.
Risk Allele
P-val 8E-10
Odds Ratio 4.87 % increase