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rs121912469

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912469(A;T)
Make rs121912469(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132489457
GeneIRF1
is asnp
is mentioned by
dbSNPrs121912469
ebirs121912469
HLIrs121912469
Exacrs121912469
Varsomers121912469
Maprs121912469
PheGenIrs121912469
hapmaprs121912469
1000 genomesrs121912469
hgdprs121912469
ensemblrs121912469
gopubmedrs121912469
geneviewrs121912469
scholarrs121912469
googlers121912469
pharmgkbrs121912469
gwascentralrs121912469
openSNPrs121912469
23andMers121912469
23andMe allrs121912469
SNP Nexus

SNPshotrs121912469
SNPdbers121912469
MSV3drs121912469
GWAS Ctlgrs121912469
Max Magnitude0
OMIM147575
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121912469(T;T)
Alt rs121912469(T;T)
Reference rs121912469(A;A)
Significance Pathogenic
Disease Neoplasm of stomach
Variation info
Gene IRF1
CLNDBN Neoplasm of stomach
Reversed 1
HGVS NC_000005.9:g.131825149T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015840.4,