Variant (rsID / SNP)
rs2242665
rs2242665 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC44A4. Location: chromosome 6, position 31,839,309. The table records no clinical significance for this variant.
Reference-table entries
SLC44A4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:31839309
- HGVS
- NM_025257.3,c.559G>A,p.Val187Ile
- Allele change
- Missense_V111I
Associated conditions / phenotypes
Malaria
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.