Variant (rsID / SNP)
rs74203920
rs74203920 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AIRE. Location: chromosome 21, position 45,714,294. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
AIREBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 21:45714294
- Cytoband
- 21q22.3
- HGVS
- NM_000383.4(AIRE):c.1411C>T (p.Arg471Cys)
- Allele change
- Missense_R471C
Associated conditions / phenotypes
Polyglandular autoimmune syndrome, type 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.