Variant (rsID / SNP)
rs191826554
rs191826554 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MYD88. Location: chromosome 3, position 38,182,019. Clinical significance in the table: Benign.
Reference-table entries
MYD88Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:38182019
- Cytoband
- 3p22.2
- HGVS
- NM_002468.5(MYD88):c.604A>C (p.Thr202Pro)
- Allele change
- Silent
Associated conditions / phenotypes
Pyogenic bacterial infections due to MyD88 deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.