Variant (rsID / SNP)

rs137852491

rs137852491 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HPRT1. Clinical significance in the table: Pathogenic.

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Reference-table entries

HPRT1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: Xq26.2
HGVS: NM_000194.3(HPRT1):c.134G>A (p.Arg45Lys)
Allele change: Missense_R45K

Associated conditions / phenotypes

Lesch-Nyhan syndrome

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.