Variant (rsID / SNP)
rs868891
rs868891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MON1A. Location: chromosome 3, position 49,949,071. The table records no clinical significance for this variant.
Reference-table entries
MON1ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:49949071
- HGVS
- NM_032355.4,c.501T>C,p.Pro167Pro
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.