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rs3859866

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3859866(C;G)
Make rs3859866(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position25770933
GeneMYO18B
is asnp
is mentioned by
dbSNPrs3859866
ebirs3859866
HLIrs3859866
Exacrs3859866
Varsomers3859866
Maprs3859866
PheGenIrs3859866
hapmaprs3859866
1000 genomesrs3859866
hgdprs3859866
ensemblrs3859866
gopubmedrs3859866
geneviewrs3859866
scholarrs3859866
googlers3859866
pharmgkbrs3859866
gwascentralrs3859866
openSNPrs3859866
23andMers3859866
23andMe allrs3859866
SNP Nexus

SNPshotrs3859866
SNPdbers3859866
MSV3drs3859866
GWAS Ctlgrs3859866
GMAF0.05556
Max Magnitude0
? (C;C) (C;G) (G;G) 28


Venter snp
Source plos
Gene MYO18B
allele C
frequency 0.983
sift TOLERATED
HuRef 1103691019309
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-W547C
aa_change Trp547Cys
aa_change_short W547C
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.978274
summary