Gene entry

NCAPH2

non-SMC condensin II complex subunit H2

Chromosome: 22
Cytoband: 22q13.33
Variants (rsID): 8

NCAPH2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q13.33). Its official name is “non-SMC condensin II complex subunit H2”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs74315511Pathogenicsingle nucleotide variantCardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1|Myopia 6|Severe global developmental delay|Seizure|Toe walking

Other listed variants

rs140524
rs6010121
rs17850507
rs73172241
rs75276302
rs112793292
rs115920265

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.