Variant (rsID / SNP)
rs2284934
rs2284934 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLF7. Location: chromosome 2, position 207,998,800. The table records no clinical significance for this variant.
Reference-table entries
KLF7Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:207998800
- HGVS
- NM_001270944.2,c.9G>A,p.Pro3Pro
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
