Variant (rsID / SNP)

rs144225009

rs144225009 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DLG3. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DLG3Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xq13.1
HGVS: NM_021120.4(DLG3):c.429C>T (p.Phe143=)
Allele change: Synonymous_F143F

Associated conditions / phenotypes

History of neurodevelopmental disorder

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.