Variant (rsID / SNP)
rs3785522
rs3785522 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBCD. Location: chromosome 17, position 80,895,933. The table records no clinical significance for this variant.
Reference-table entries
TBCDNot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:80895933
- HGVS
- NM_005993.5,c.3290A>G,p.Glu1097Gly
- Allele change
- Missense_E1097G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.