Variant (rsID / SNP)
rs1025806
rs1025806 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TEX38. Location: chromosome 1, position 47,139,103. The table records no clinical significance for this variant.
Reference-table entries
TEX38Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:47139103
- HGVS
- NM_001145474.4,c.596C>T,p.Ala199Val
- Allele change
- Missense_A199V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.