Variant (rsID / SNP)
rs1805107
rs1805107 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDX2. Location: chromosome 13, position 28,537,317. The table records no clinical significance for this variant.
Reference-table entries
CDX2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 13:28537317
- HGVS
- NM_001265.6,c.877C>T,p.Pro293Ser
- Allele change
- Missense_P293S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.