Variant (rsID / SNP)
rs7304723
rs7304723 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AICDA. Location: chromosome 12, position 8,755,852. Clinical significance in the table: Benign.
Reference-table entries
AICDABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:8755852
- Cytoband
- 12p13.31
- HGVS
- NM_020661.4(AICDA):c.*1028C>T
- Allele change
- Silent
Associated conditions / phenotypes
Hyper-IgM syndrome type 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.