Variant (rsID / SNP)
rs260462
rs260462 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF544. Location: chromosome 19, position 58,774,071. The table records no clinical significance for this variant.
Reference-table entries
ZNF544Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:58774071
- HGVS
- NM_001387410.1,c.2261A>G,p.Gln754Arg
- Allele change
- Missense_Q700R
Associated conditions / phenotypes
Silent|Missense_Q700R|Silent|Silent|Missense_Q700R|Silent|Missense_Q672R|Missense_Q465R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.