Variant (rsID / SNP)
rs2270576
rs2270576 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNF8. Location: chromosome 17, position 47,007,963. The table records no clinical significance for this variant.
Reference-table entries
SNF8Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:47007963
- HGVS
- NM_007241.4,c.651G>A,p.Leu217Leu
- Allele change
- Synonymous_L216L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.