Variant (rsID / SNP)
rs3178137
rs3178137 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OBP2A. Location: chromosome 9, position 138,440,562. The table records no clinical significance for this variant.
Reference-table entries
OBP2ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 9:138440562
- HGVS
- NM_001293193.2,c.328C>T,p.Pro110Ser
- Allele change
- Synonymous_I154I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.