Variant (rsID / SNP)
rs429608
rs429608 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SKIV2L. Location: chromosome 6, position 31,930,462. The table records no clinical significance for this variant.
Reference-table entries
SKIV2LNot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:31930462
- Cytoband
- 6p21.33
- HGVS
- NM_006929.5(SKIV2L):c.1212-29G>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
