Variant (rsID / SNP)
rs3989369
rs3989369 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPL39. Location: chromosome 21, position 26,978,950. The table records no clinical significance for this variant.
Reference-table entries
MRPL39Not classified
- Variant type
- missense_variant
- Chromosome / position
- 21:26978950
- HGVS
- NM_080794.4,c.91T>C,p.Ser31Pro
- Allele change
- Missense_S31P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.