Variant (rsID / SNP)
rs2301816
rs2301816 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OSBP2. Location: chromosome 22, position 31,266,546. The table records no clinical significance for this variant.
Reference-table entries
OSBP2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 22:31266546
- HGVS
- NM_030758.4,c.984T>C,p.Ala328Ala
- Allele change
- Synonymous_A163A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.