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rs121912470

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912470(C;C)
Make rs121912470(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132489448
GeneIRF1
is asnp
is mentioned by
dbSNPrs121912470
ebirs121912470
HLIrs121912470
Exacrs121912470
Varsomers121912470
Maprs121912470
PheGenIrs121912470
hapmaprs121912470
1000 genomesrs121912470
hgdprs121912470
ensemblrs121912470
gopubmedrs121912470
geneviewrs121912470
scholarrs121912470
googlers121912470
pharmgkbrs121912470
gwascentralrs121912470
openSNPrs121912470
23andMers121912470
23andMe allrs121912470
SNP Nexus

SNPshotrs121912470
SNPdbers121912470
MSV3drs121912470
GWAS Ctlgrs121912470
Max Magnitude0
OMIM147575
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912470(C;C)
Alt rs121912470(C;C)
Reference rs121912470(T;T)
Significance Pathogenic
Disease Non-small cell lung cancer
Variation info
Gene IRF1
CLNDBN Non-small cell lung cancer
Reversed 1
HGVS NC_000005.9:g.131825140A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000015841.25,