Variant (rsID / SNP)
rs3758938
rs3758938 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TBX10. Location: chromosome 11, position 67,402,362. The table records no clinical significance for this variant.
Reference-table entries
TBX10Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:67402362
- HGVS
- NM_005995.5,c.302A>C,p.Lys101Thr
- Allele change
- Missense_K101T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.