{{Rsnum
|rsid=4371677
|Gene=HOPX
|Chromosome=4
|position=56650730
|Orientation=plus
|GMAF=0.4931
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HOPX
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 20.5 | 45.5 | 33.9
| HCB | 19.9 | 45.6 | 34.6
| JPT | 15.9 | 36.3 | 47.8
| YRI | 48.3 | 41.5 | 10.2
| ASW | 43.9 | 43.9 | 12.3
| CHB | 19.9 | 45.6 | 34.6
| CHD | 28.0 | 47.7 | 24.3
| GIH | 15.8 | 39.6 | 44.6
| LWK | 50.9 | 37.3 | 11.8
| MEX | 8.8 | 49.1 | 42.1
| MKK | 23.2 | 57.4 | 19.4
| TSI | 22.5 | 50.0 | 27.5
| HapMapRevision=28
}}

{{Venter SNP
|rsid=4371677
|allele=A
|frequency=0.442
|uid=1103654417252
|type=heterozygous_SNP
|hugo=HOP_HUMAN
|ensembl gene=ENSG00000171476
|ensembl transcript=ENST00000317745
|sift=
|disease=Defects in HOP may be a cause of various types of cancer, such as lung cancer, choriocarcinoma, head and neck squamous cell carcinoma and oral squamous cell carcinoma.
}}

{{GET Evidence
|gene=HOPX
|aa_change=Pro94Leu
|aa_change_short=P94L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4371677
|n_genomes=1
|n_genomes_annotated=0
|n_haplomes=2
|n_articles=0
|n_articles_annotated=0
|nblosum100=7
|autoscore=1
|webscore=N
}}

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