Variant (rsID / SNP)

rs146925326

rs146925326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALG13. Clinical significance in the table: Benign.

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Reference-table entries

ALG13Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq23
HGVS: NM_001099922.3(ALG13):c.183C>T (p.Tyr61=)
Allele change: Synonymous_Y61Y

Associated conditions / phenotypes

History of neurodevelopmental disorder|Developmental and epileptic encephalopathy, 36

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.