{{Rsnum
|rsid=7338333
|Gene=ING1
|Chromosome=13
|position=110715817
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=G
|GMAF=0
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ING1
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 100.0 | 0.0 | 0.0
| HCB | 100.0 | 0.0 | 0.0
| JPT | 97.2 | 2.8 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 98.2 | 1.8 | 0.0
| GIH | 97.9 | 2.1 | 0.0
| LWK | 95.3 | 4.7 | 0.0
| MEX | 96.4 | 3.6 | 0.0
| MKK | 98.0 | 2.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=7338333
|allele=G
|frequency=1
|uid=1103649336192
|type=homozygous_SNP
|hugo=ING1
|ensembl gene=ENSG00000153487
|ensembl transcript=ENST00000283537
|sift=
|disease=Defects in ING1 are a cause of squamous cell carcinoma of the head and neck (HNSCC) (MIM:275355).
}}

{{GET Evidence
|gene=ING1
|aa_change=Leu125Arg
|aa_change_short=L125R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7338333
|overall_frequency_n=9891
|overall_frequency_d=9900
|overall_frequency=0.999091
|n_genomes=50
|n_genomes_annotated=0
|n_haplomes=100
|n_articles=0
|n_articles_annotated=0
|nblosum100=6
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}