Variant (rsID / SNP)
rs2075117
rs2075117 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC80. Location: chromosome 2, position 210,843,383. The table records no clinical significance for this variant.
Reference-table entries
UNC80Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:210843383
- HGVS
- NM_001371986.1,c.9069G>A,p.Gln3023Gln
- Allele change
- Synonymous_Q2957Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
