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rs5761268

From SNPedia

Orientationplus
Stabilizedplus
Make rs5761268(A;A)
Make rs5761268(A;C)
Make rs5761268(C;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position25843883
GeneMYO18B
is asnp
is mentioned by
dbSNPrs5761268
ebirs5761268
HLIrs5761268
Exacrs5761268
Varsomers5761268
Maprs5761268
PheGenIrs5761268
hapmaprs5761268
1000 genomesrs5761268
hgdprs5761268
ensemblrs5761268
gopubmedrs5761268
geneviewrs5761268
scholarrs5761268
googlers5761268
pharmgkbrs5761268
gwascentralrs5761268
openSNPrs5761268
23andMers5761268
23andMe allrs5761268
SNP Nexus

SNPshotrs5761268
SNPdbers5761268
MSV3drs5761268
GWAS Ctlgrs5761268
GMAF0.27
Max Magnitude
? (A;A) (A;C) (C;C) 28


Venter snp
Source plos
Gene MYO18B
allele A
frequency 0.7
sift TOLERATED
HuRef 1103691019489
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-H1119Q
aa_change His1119Gln
aa_change_short H1119Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.641426
summary