Variant (rsID / SNP)
rs7575
rs7575 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPL40. Location: chromosome 22, position 19,423,250. The table records no clinical significance for this variant.
Reference-table entries
MRPL40Not classified
- Variant type
- missense_variant
- Chromosome / position
- 22:19423250
- HGVS
- NM_003776.4,c.386G>A,p.Arg129His
- Allele change
- Missense_R129H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.