Variant (rsID / SNP)
rs35715176
rs35715176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KANSL3. Location: chromosome 2, position 97,271,090. The table records no clinical significance for this variant.
Reference-table entries
KANSL3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:97271090
- HGVS
- NM_001349256.2,c.1978C>T,p.Pro660Ser
- Allele change
- Silent
Associated conditions / phenotypes
Silent|Missense_P432S|Missense_P660S|Missense_P660S|Silent|Missense_P449S|Missense_P573S|Missense_P660S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.