Variant (rsID / SNP)
rs6972561
rs6972561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GTPBP10. Location: chromosome 7, position 89,982,132. The table records no clinical significance for this variant.
Reference-table entries
GTPBP10Not classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 7:89982132
- HGVS
- NM_033107.4,c.36T>C,p.Tyr12Tyr
- Allele change
- Synonymous_Y12Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.