Variant (rsID / SNP)

rs13263632

rs13263632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASAH1. Location: chromosome 8, position 17,942,204. Clinical significance in the table: Benign.

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Reference-table entries

ASAH1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:17942204
Cytoband: 8p22
HGVS: NM_004315.6(ASAH1):c.107G>A (p.Ser36Asn)
Allele change: Missense_S36N

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.