Variant (rsID / SNP)

rs201503661

rs201503661 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC26A1, IDUA. Location: chromosome 4, position 983,042. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SLC26A1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 4:983042
Cytoband: 4p16.3
HGVS: NM_022042.4(SLC26A1):c.1685C>T (p.Thr562Met)
Allele change: Silent

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.