Variant (rsID / SNP)
rs2304968
rs2304968 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLFN12L. Location: chromosome 17, position 33,805,150. The table records no clinical significance for this variant.
Reference-table entries
SLFN12LNot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:33805150
- HGVS
- NM_001363830.2,c.1220A>G,p.Tyr407Cys
- Allele change
- Missense_Y412C
Associated conditions / phenotypes
Lung Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.