Variant (rsID / SNP)
rs10015804
rs10015804 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RWDD4. Location: chromosome 4, position 184,570,715. The table records no clinical significance for this variant.
Reference-table entries
RWDD4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:184570715
- HGVS
- NM_152682.4,c.370A>C,p.Ile124Leu
- Allele change
- Missense_I61L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.