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rs121909251

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121909251(A;G)
Make rs121909251(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110719739
GeneING1
is asnp
is mentioned by
dbSNPrs121909251
ebirs121909251
HLIrs121909251
Exacrs121909251
Varsomers121909251
Maprs121909251
PheGenIrs121909251
hapmaprs121909251
1000 genomesrs121909251
hgdprs121909251
ensemblrs121909251
gopubmedrs121909251
geneviewrs121909251
scholarrs121909251
googlers121909251
pharmgkbrs121909251
gwascentralrs121909251
openSNPrs121909251
23andMers121909251
23andMe allrs121909251
SNP Nexus

SNPshotrs121909251
SNPdbers121909251
MSV3drs121909251
GWAS Ctlgrs121909251
Max Magnitude0
OMIM601566
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121909251(G;G)
Alt rs121909251(G;G)
Reference rs121909251(A;A)
Significance Pathogenic
Disease Squamous cell carcinoma of the head and neck
Variation info
Gene ING1
CLNDBN Squamous cell carcinoma of the head and neck
Reversed 0
HGVS NC_000013.10:g.111372086A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008534.4,