Gene entry
KIF7
kinesin family member 7
- Chromosome
- 15
- Cytoband
- 15q26.1
- Variants (rsID)
- 20
KIF7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q26.1). Its official name is “kinesin family member 7”. The reference table lists 20 variants (rsID) for this gene.
Clinically classified variants
15 reference-table entries with clinical significance.
- rs116823950Benignsingle nucleotide variantAcrocallosal syndrome
- rs141865394Benignsingle nucleotide variantAcrocallosal syndrome
- rs145049849Benignsingle nucleotide variantAcrocallosal syndrome
- rs3803530Benignsingle nucleotide variantAcrocallosal syndrome|Multiple epiphyseal dysplasia, Al-Gazali type|Hydrolethalus syndrome 2
- rs527804875Benignsingle nucleotide variantAcrocallosal syndrome
- rs8179065Benignsingle nucleotide variantAcrocallosal syndrome|Multiple epiphyseal dysplasia, Al-Gazali type|Hydrolethalus syndrome 2
- rs138354681Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome|Nephronophthisis
- rs138410949Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome|Intellectual disability
- rs141028210Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome
- rs141514601Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome
- rs143877028Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome|Multiple epiphyseal dysplasia, Al-Gazali type
- rs150248985Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome
- rs201251064Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome
- rs398124613Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome
- rs79532879Conflicting interpretationssingle nucleotide variantAcrocallosal syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.