Variant (rsID / SNP)
rs10255061
rs10255061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IQUB. Location: chromosome 7, position 123,152,019. The table records no clinical significance for this variant.
Reference-table entries
IQUBNot classified
- Variant type
- missense_variant
- Chromosome / position
- 7:123152019
- HGVS
- NM_001282855.2,c.376G>A,p.Val126Met
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.