Variant (rsID / SNP)
rs2279073
rs2279073 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF227. Location: chromosome 19, position 44,739,303. The table records no clinical significance for this variant.
Reference-table entries
ZNF227Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:44739303
- HGVS
- NM_001289166.2,c.720T>C,p.Asn240Asn
- Allele change
- Synonymous_N212N
Associated conditions / phenotypes
Synonymous_N189N|Synonymous_N189N|Synonymous_N161N|Synonymous_N240N
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.