Variant (rsID / SNP)

rs180177152

rs180177152 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRPS1. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PRPS1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Cytoband: Xq22.3
HGVS: NM_002764.4(PRPS1):c.259G>A (p.Ala87Thr)
Allele change: Silent

Associated conditions / phenotypes

Hearing loss, X-linked 1|Charcot-Marie-Tooth Neuropathy X

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.