Variant (rsID / SNP)
rs1048408
rs1048408 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR87. Location: chromosome 3, position 151,011,969. The table records no clinical significance for this variant.
Reference-table entries
GPR87Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:151011969
- HGVS
- NM_023915.4,c.1065C>T,p.Tyr355Tyr
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.