Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909252

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121909252(A;A)
Make rs121909252(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position110719667
GeneING1
is asnp
is mentioned by
dbSNPrs121909252
ebirs121909252
HLIrs121909252
Exacrs121909252
Varsomers121909252
Maprs121909252
PheGenIrs121909252
hapmaprs121909252
1000 genomesrs121909252
hgdprs121909252
ensemblrs121909252
gopubmedrs121909252
geneviewrs121909252
scholarrs121909252
googlers121909252
pharmgkbrs121909252
gwascentralrs121909252
openSNPrs121909252
23andMers121909252
23andMe allrs121909252
SNP Nexus

SNPshotrs121909252
SNPdbers121909252
MSV3drs121909252
GWAS Ctlgrs121909252
Max Magnitude0
OMIM601566
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909252(A;A)
Alt rs121909252(A;A)
Reference rs121909252(C;C)
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.111372014C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008535.4,