Variant (rsID / SNP)

rs74882337

rs74882337 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AASS. Location: chromosome 7, position 121,733,190. Clinical significance in the table: Likely benign.

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Reference-table entries

AASSLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:121733190
Cytoband: 7q31.32
HGVS: NM_005763.4(AASS):c.1678C>T (p.Pro560Ser)
Allele change: Missense_P560S

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.