Variant (rsID / SNP)
rs2286587
rs2286587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MXRA7. Location: chromosome 17, position 74,684,401. The table records no clinical significance for this variant.
Reference-table entries
MXRA7Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:74684401
- HGVS
- NM_001387276.1,c.329A>G,p.His110Arg
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.