Variant (rsID / SNP)
rs3747552
rs3747552 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMCC3. Location: chromosome 12, position 94,976,084. The table records no clinical significance for this variant.
Reference-table entries
TMCC3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:94976084
- HGVS
- NM_020698.4,c.309A>G,p.Ala103Ala
- Allele change
- Synonymous_A103A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.