Variant (rsID / SNP)
rs10916668
rs10916668 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OTUD3. Location: chromosome 1, position 20,233,086. The table records no clinical significance for this variant.
Reference-table entries
OTUD3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:20233086
- HGVS
- NM_015207.2,c.997G>A,p.Ala333Thr
- Allele change
- Missense_A333T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.