Gene entry

ORC6

origin recognition complex subunit 6

Chromosome: 16
Cytoband: 16q11.2
Variants (rsID): 5

ORC6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q11.2). Its official name is “origin recognition complex subunit 6”. The reference table lists 5 variants (rsID) for this gene.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Clinically classified variants

3 reference-table entries with clinical significance.

rs34343511Benignsingle nucleotide variantMeier-Gorlin syndrome 3
rs144065502Conflicting interpretationssingle nucleotide variantMeier-Gorlin syndrome|Parkinson Disease, Dominant|Meier-Gorlin syndrome 3
rs200089121Likely pathogenicsingle nucleotide variantMeier-Gorlin syndrome 3

Other listed variants

rs78674672
rs143913118

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.