Variant (rsID / SNP)

rs398124379

rs398124379 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NSD1. Location: chromosome 5, position 176,694,695. Clinical significance in the table: Pathogenic.

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Reference-table entries

NSD1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 5:176694695
Cytoband: 5q35.3
HGVS: NM_022455.5(NSD1):c.5279_5282del (p.Val1760fs)

Associated conditions / phenotypes

Sotos syndrome 1

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.