Variant (rsID / SNP)
rs2073145
rs2073145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZBP1. Location: chromosome 20, position 56,190,634. The table records no clinical significance for this variant.
Reference-table entries
ZBP1Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 20:56190634
- HGVS
- NM_030776.3,c.262G>A,p.Glu88Lys
- Allele change
- Missense_E88K
Associated conditions / phenotypes
Missense_E88K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.