Variant (rsID / SNP)
rs5992854
rs5992854 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MICAL3. Location: chromosome 22, position 18,300,240. The table records no clinical significance for this variant.
Reference-table entries
MICAL3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 22:18300240
- HGVS
- NM_015241.3,c.5187A>G,p.Leu1729Leu
- Allele change
- Synonymous_L1729L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.