Variant (rsID / SNP)
rs10512472
rs10512472 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLFN14. Location: chromosome 17, position 33,884,804. The table records no clinical significance for this variant.
Reference-table entries
SLFN14Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:33884804
- HGVS
- NM_001129820.2,c.278A>G,p.Gln93Arg
- Allele change
- Missense_Q93R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.