Variant (rsID / SNP)
rs112579822
rs112579822 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AAAS. Location: chromosome 12, position 53,701,866. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
AAASConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:53701866
- Cytoband
- 12q13.13
- HGVS
- NM_015665.6(AAAS):c.1301G>A (p.Arg434Gln)
- Allele change
- Missense_R401Q
Associated conditions / phenotypes
Glucocorticoid deficiency with achalasia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.