Gene entry

RHOT2

ras homolog family member T2

Chromosome

16

Cytoband

16p13.3

Variants (rsID)

7

RHOT2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “ras homolog family member T2”. The reference table lists 7 variants (rsID) for this gene.

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