{{Rsnum
|rsid=1494961
|Gene=HELQ
|Chromosome=4
|position=83453327
|Orientation=plus
|GMAF=0.3737
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HELQ
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 16.8 | 56.6 | 26.5
| HCB | 12.0 | 36.1 | 51.9
| JPT | 13.5 | 48.6 | 37.8
| YRI | 2.0 | 25.2 | 72.8
| ASW | 10.5 | 36.8 | 52.6
| CHB | 12.0 | 36.1 | 51.9
| CHD | 12.0 | 42.6 | 45.4
| GIH | 17.5 | 48.5 | 34.0
| LWK | 0.0 | 31.8 | 68.2
| MEX | 13.8 | 37.9 | 48.3
| MKK | 1.9 | 46.2 | 51.9
| TSI | 29.0 | 52.0 | 19.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21437268
|Title=A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium
|OA=1
}}

{{GET Evidence
|gene=HELQ
|aa_change=Val306Ile
|aa_change_short=V306I
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1494961
|overall_frequency_n=6372
|overall_frequency_d=10758
|overall_frequency=0.592303
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=75
|n_articles=0
|n_articles_annotated=0
|nblosum100=-4
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23430454
|Title=Genetic variants at 4q21, 4q23 and 12q24 are associated with esophageal squamous cell carcinoma risk in a Chinese population
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}