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rs5761170

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs5761170(C;T)
Make rs5761170(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position25777694
GeneMYO18B
is asnp
is mentioned by
dbSNPrs5761170
dbSNP (old)rs5761170
ClinGenrs5761170
ebirs5761170
HLIrs5761170
Exacrs5761170
Gnomadrs5761170
Varsomers5761170
Maprs5761170
PheGenIrs5761170
Biobankrs5761170
1000 genomesrs5761170
hgdprs5761170
ensemblrs5761170
gopubmedrs5761170
geneviewrs5761170
scholarrs5761170
googlers5761170
pharmgkbrs5761170
gwascentralrs5761170
openSNPrs5761170
23andMers5761170
23andMe allrs5761170
SNP Nexus

SNPshotrs5761170
SNPdbers5761170
MSV3drs5761170
GWAS Ctlgrs5761170
GMAF0.08356
Max Magnitude0
? (C;C) (C;T) (T;T) 28


Venter snp
Source plos
Gene MYO18B
allele C
frequency 0.983
sift TOLERATED
HuRef 1103691019318
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-W661R
aa_change Trp661Arg
aa_change_short W661R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.972201
summary