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Variant (rsID / SNP)

rs184639841

TBC1D24

rs184639841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBC1D24. Location: chromosome 16, position 2,550,292. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TBC1D24Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
16:2550292
Cytoband
16p13.3
HGVS
NM_001199107.2(TBC1D24):c.1326C>T (p.Tyr442=)
Allele change
Synonymous_Y442Y

Associated conditions / phenotypes

Familial infantile myoclonic epilepsy|Seizure|Caused by mutation in the TBC1 domain family, member 24|Developmental and epileptic encephalopathy, 1|Autosomal dominant nonsyndromic hearing loss 65

Public references

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