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rs121909250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121909250(C;C)
Make rs121909250(C;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position110719736
GeneING1
is asnp
is mentioned by
dbSNPrs121909250
ebirs121909250
HLIrs121909250
Exacrs121909250
Varsomers121909250
Maprs121909250
PheGenIrs121909250
hapmaprs121909250
1000 genomesrs121909250
hgdprs121909250
ensemblrs121909250
gopubmedrs121909250
geneviewrs121909250
scholarrs121909250
googlers121909250
pharmgkbrs121909250
gwascentralrs121909250
openSNPrs121909250
23andMers121909250
23andMe allrs121909250
SNP Nexus

SNPshotrs121909250
SNPdbers121909250
MSV3drs121909250
GWAS Ctlgrs121909250
Max Magnitude0
OMIM601566
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909250(C;C)
Alt rs121909250(C;C)
Reference rs121909250(G;G)
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.111372083G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008533.4,