Variant (rsID / SNP)
rs321612
rs321612 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLFN14. Location: chromosome 17, position 33,881,631. The table records no clinical significance for this variant.
Reference-table entries
SLFN14Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:33881631
- HGVS
- NM_001129820.2,c.1153A>G,p.Lys385Glu
- Allele change
- Missense_K385E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.