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rs121909071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121909071(C;T)
Make rs121909071(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2918030
GeneSLC22A18
is asnp
is mentioned by
dbSNPrs121909071
ebirs121909071
HLIrs121909071
Exacrs121909071
Varsomers121909071
Maprs121909071
PheGenIrs121909071
hapmaprs121909071
1000 genomesrs121909071
hgdprs121909071
ensemblrs121909071
gopubmedrs121909071
geneviewrs121909071
scholarrs121909071
googlers121909071
pharmgkbrs121909071
gwascentralrs121909071
openSNPrs121909071
23andMers121909071
23andMe allrs121909071
SNP Nexus

SNPshotrs121909071
SNPdbers121909071
MSV3drs121909071
GWAS Ctlgrs121909071
Max Magnitude0
OMIM602631
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909071(T;T)
Alt rs121909071(T;T)
Reference rs121909071(C;C)
Significance Pathogenic
Disease Lung cancer
Variation info
Gene SLC22A18
CLNDBN Lung cancer
Reversed 0
HGVS NC_000011.9:g.2939260C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007393.4,