Variant (rsID / SNP)
rs4790706
rs4790706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VMO1. Location: chromosome 17, position 4,689,572. The table records no clinical significance for this variant.
Reference-table entries
VMO1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:4689572
- HGVS
- NM_182566.3,c.76A>G,p.Thr26Ala
- Allele change
- Missense_T26A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.