Variant (rsID / SNP)
rs1800547
rs1800547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAPT. Location: chromosome 17, position 44,051,846. Clinical significance in the table: Benign.
Reference-table entries
MAPTBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:44051846
- Cytoband
- 17q21.31
- HGVS
- NM_001377265.1(MAPT):c.220+2535A>G
- Allele change
- Silent
Associated conditions / phenotypes
MAPT-Related Spectrum Disorders|Frontotemporal dementia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.