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Variant (rsID / SNP)

rs74315476

ARSA

rs74315476 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARSA. Location: chromosome 22, position 51,064,103. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

ARSAPathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
22:51064103
Cytoband
22q13.33
HGVS
NM_000487.6(ARSA):c.1114C>T (p.Arg372Trp)
Allele change
Missense_R286W

Associated conditions / phenotypes

Metachromatic leukodystrophy, severe|Metachromatic leukodystrophy

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.