Variant (rsID / SNP)
rs9907142
rs9907142 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OSBPL7. Location: chromosome 17, position 45,885,687. The table records no clinical significance for this variant.
Reference-table entries
OSBPL7Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:45885687
- HGVS
- NM_145798.3,c.2499T>C,p.Tyr833Tyr
- Allele change
- Synonymous_Y833Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.