Variant (rsID / SNP)
rs238209
rs238209 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNFX1. Location: chromosome 20, position 47,865,509. The table records no clinical significance for this variant.
Reference-table entries
ZNFX1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 20:47865509
- HGVS
- NM_021035.3,c.4052C>T,p.Thr1351Ile
- Allele change
- Missense_T1351I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
