Variant (rsID / SNP)
rs1054485
rs1054485 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF415. Location: chromosome 19, position 53,612,757. The table records no clinical significance for this variant.
Reference-table entries
ZNF415Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:53612757
- HGVS
- NM_001352130.2,c.772A>C,p.Ile258Leu
- Allele change
- Missense_I229L
Associated conditions / phenotypes
Missense_I181L|Silent|Missense_I181L|Missense_I258L|Missense_I181L|Missense_I181L|Missense_I168L|Missense_I217L|Missense_I229L|Missense_I217L|Missense_I193L|Missense_I193L|Missense_I193L|Missense_I168L|Missense_I168L|Missense_I181L|Missense_I229L|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.