Variant (rsID / SNP)
rs2273454
rs2273454 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRM3, GLOD4. Location: chromosome 17, position 685,640. The table records no clinical significance for this variant.
Reference-table entries
MRM3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:685640
- HGVS
- NM_018146.4,c.22G>T,p.Ala8Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
