Gene entry
NIPA1
NIPA magnesium transporter 1
- Chromosome
- 15
- Cytoband
- 15q11.2
- Variants (rsID)
- 24
NIPA1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q11.2). Its official name is “NIPA magnesium transporter 1”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs11263683Benignsingle nucleotide variantHereditary spastic paraplegia 6|Hereditary spastic paraplegia
- rs3812923Benignsingle nucleotide variantHereditary spastic paraplegia 6
- rs7181789Benignsingle nucleotide variantHereditary spastic paraplegia 6
- rs73412681Benignsingle nucleotide variantHereditary spastic paraplegia 6
- rs139372534Conflicting interpretationssingle nucleotide variantHereditary spastic paraplegia 6|Hereditary spastic paraplegia
- rs199818530Likely benignsingle nucleotide variantHereditary spastic paraplegia 6
- rs104894490Pathogenicsingle nucleotide variantHereditary spastic paraplegia 6
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.