Variant (rsID / SNP)
rs1263811
rs1263811 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SALL2. Location: chromosome 14, position 21,993,498. The table records no clinical significance for this variant.
Reference-table entries
SALL2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 14:21993498
- HGVS
- NM_005407.3,c.364C>T,p.Pro122Ser
- Allele change
- Missense_P120S
Associated conditions / phenotypes
Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.