Variant (rsID / SNP)
rs11546406
rs11546406 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPL44. Location: chromosome 2, position 224,824,484. Clinical significance in the table: Benign.
Reference-table entries
MRPL44Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:224824484
- Cytoband
- 2q36.1
- HGVS
- NM_022915.5(MRPL44):c.413C>T (p.Thr138Ile)
- Allele change
- Missense_T138I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.