Variant (rsID / SNP)
rs2306392
rs2306392 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MDM1. Location: chromosome 12, position 68,707,287. The table records no clinical significance for this variant.
Reference-table entries
MDM1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:68707287
- HGVS
- NM_001354969.2,c.1685C>T,p.Pro562Leu
- Allele change
- Missense_P282L
Associated conditions / phenotypes
Missense_P512L|Missense_P282L|Missense_P282L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.