Variant (rsID / SNP)
rs9908756
rs9908756 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to METRNL. Location: chromosome 17, position 81,043,039. The table records no clinical significance for this variant.
Reference-table entries
METRNLNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:81043039
- HGVS
- NM_001004431.3,c.396A>G,p.Pro132Pro
- Allele change
- Synonymous_P132P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.