Variant (rsID / SNP)

rs6151425

rs6151425 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARSA. Location: chromosome 22, position 51,064,068. The table records no clinical significance for this variant.

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Reference-table entries

ARSANot classified

Variant type: single nucleotide variant
Chromosome / position: 22:51064068
Cytoband: 22q13.33
HGVS: NM_000487.6(ARSA):c.1149C>G (p.Asp383Glu)
Allele change: Synonymous_D297D

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.