Variant (rsID / SNP)

rs180177153

rs180177153 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRPS1. Clinical significance in the table: Pathogenic.

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Reference-table entries

PRPS1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: Xq22.3
HGVS: NM_002764.4(PRPS1):c.869T>C (p.Ile290Thr)
Allele change: Missense_I86T

Associated conditions / phenotypes

Hearing loss, X-linked 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.