Variant (rsID / SNP)
rs41270133
rs41270133 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLHL9. Location: chromosome 9, position 21,333,254. The table records no clinical significance for this variant.
Reference-table entries
KLHL9Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 9:21333254
- HGVS
- NM_018847.4,c.1605A>G,p.Gln535Gln
- Allele change
- Synonymous_Q535Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.