Variant (rsID / SNP)

rs17651549

rs17651549 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAPT. Location: chromosome 17, position 44,061,278. Clinical significance in the table: Benign.

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Reference-table entries

MAPTBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:44061278
Cytoband: 17q21.31
HGVS: NM_001377265.1(MAPT):c.1333C>T (p.Arg445Trp)
Allele change: Missense_R370W

Associated conditions / phenotypes

Frontotemporal dementia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.