Variant (rsID / SNP)
rs394558
rs394558 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TATDN2. Location: chromosome 3, position 10,302,172. The table records no clinical significance for this variant.
Reference-table entries
TATDN2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:10302172
- HGVS
- NM_014760.4,c.766G>A,p.Val256Ile
- Allele change
- Missense_V256I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.