Variant (rsID / SNP)
rs1051061
rs1051061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VRK2. Location: chromosome 2, position 58,316,814. The table records no clinical significance for this variant.
Reference-table entries
VRK2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:58316814
- HGVS
- NM_001130480.2,c.499A>G,p.Ile167Val
- Allele change
- Missense_I167V
Associated conditions / phenotypes
Schizophrenia|Missense_I167V|Missense_I49V|Missense_I167V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.