Variant (rsID / SNP)
rs214803
rs214803 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGM3. Location: chromosome 20, position 2,290,333. The table records no clinical significance for this variant.
Reference-table entries
TGM3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 20:2290333
- HGVS
- NM_003245.4,c.38C>A,p.Thr13Lys
- Allele change
- Missense_T13K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.