Variant (rsID / SNP)

rs121434257

rs121434257 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AIRE. Location: chromosome 21, position 45,709,569. Clinical significance in the table: Pathogenic.

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Reference-table entries

AIREPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 21:45709569
Cytoband: 21q22.3
HGVS: NM_000383.4(AIRE):c.682G>T (p.Gly228Trp)
Allele change: Missense_G228W

Associated conditions / phenotypes

Autoimmune polyglandular syndrome type 1, autosomal dominant

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.