Variant (rsID / SNP)
rs12624279
rs12624279 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOSL2. Location: chromosome 2, position 28,634,790. The table records no clinical significance for this variant.
Reference-table entries
FOSL2Not classified
- Variant type
- splice_region_variant&intron_variant
- Chromosome / position
- 2:28634790
- HGVS
- NM_005253.4,c.463-7G>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.