Variant (rsID / SNP)

rs121907986

rs121907986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HEXB. Location: chromosome 5, position 74,009,409. Clinical significance in the table: Pathogenic.

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Reference-table entries

HEXBPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 5:74009409
Cytoband: 5q13.3
HGVS: NM_000521.4(HEXB):c.850C>T (p.Arg284Ter)
Allele change: Nonsense_R59X

Associated conditions / phenotypes

Sandhoff disease, infantile form|Sandhoff disease

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.