Variant (rsID / SNP)
rs2032653
rs2032653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UTY. Location: chromosome Y, position 15,591,537. The table records no clinical significance for this variant.
Reference-table entries
UTYNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- Y:15591537
- HGVS
- NM_001400170.1,c.9C>G,p.Ser3Ser
- Allele change
- Synonymous_S3S
Associated conditions / phenotypes
Synonymous_S3S|Silent|Silent|Synonymous_S3S|Silent|Silent|Synonymous_S3S|Synonymous_S3S|Silent|Synonymous_S3S|Synonymous_S3S|Silent|Silent|Synonymous_S3S|Silent|Synonymous_S3S|Silent|Synonymous_S3S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.