Variant (rsID / SNP)
rs2997211
rs2997211 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MPP7. Location: chromosome 10, position 28,378,758. The table records no clinical significance for this variant.
Reference-table entries
MPP7Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:28378758
- HGVS
- NM_001318170.2,c.965A>G,p.Lys322Arg
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.