Variant (rsID / SNP)
rs3732401
rs3732401 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GTF2E1. Location: chromosome 3, position 120,500,093. The table records no clinical significance for this variant.
Reference-table entries
GTF2E1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:120500093
- HGVS
- NM_005513.3,c.1096C>T,p.Pro366Ser
- Allele change
- Missense_P366S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.