Variant (rsID / SNP)

rs6151429

rs6151429 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARSA. Location: chromosome 22, position 51,063,477. Clinical significance in the table: Benign; other.

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Reference-table entries

ARSABenign

Clinical significance (as recorded): Benign; other
Variant type: single nucleotide variant
Chromosome / position: 22:51063477
Cytoband: 22q13.33
HGVS: NM_000487.6(ARSA):c.*96A>G
Allele change: Silent

Associated conditions / phenotypes

Arylsulfatase A pseudodeficiency|Metachromatic leukodystrophy

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.