Variant (rsID / SNP)
rs2286656
rs2286656 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SFTA2. Location: chromosome 6, position 30,899,571. The table records no clinical significance for this variant.
Reference-table entries
SFTA2Not classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 6:30899571
- HGVS
- NM_205854.3,c.63G>A,p.Gly21Gly
- Allele change
- Synonymous_G21G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.