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

rs7338333

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs7338333(G;T)
Make rs7338333(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position110715817
GeneING1
is asnp
is mentioned by
dbSNPrs7338333
ebirs7338333
HLIrs7338333
Exacrs7338333
Varsomers7338333
Maprs7338333
PheGenIrs7338333
hapmaprs7338333
1000 genomesrs7338333
hgdprs7338333
ensemblrs7338333
gopubmedrs7338333
geneviewrs7338333
scholarrs7338333
googlers7338333
pharmgkbrs7338333
gwascentralrs7338333
openSNPrs7338333
23andMers7338333
23andMe allrs7338333
SNP Nexus

SNPshotrs7338333
SNPdbers7338333
MSV3drs7338333
GWAS Ctlgrs7338333
GMAF0
Max Magnitude0
? (G;G) (G;T) (T;T) 28
Venter snp
Source plos
Gene ING1
allele G
frequency 1
sift
HuRef 1103649336192
Disease Association Defects in ING1 are a cause of squamous cell carcinoma of the head and neck (HNSCC) (MIM:275355).



GET Evidence
ING1-L125R
aa_change Leu125Arg
aa_change_short L125R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.999091
summary