Variant (rsID / SNP)
rs2032654
rs2032654 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UTY. Location: chromosome Y, position 15,467,824. The table records no clinical significance for this variant.
Reference-table entries
UTYNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- Y:15467824
- HGVS
- NM_001400170.1,c.1488T>C,p.Ser496Ser
- Allele change
- Synonymous_S435S
Associated conditions / phenotypes
Synonymous_S496S|Silent|Silent|Synonymous_S496S|Silent|Silent|Synonymous_S451S|Synonymous_S451S|Silent|Synonymous_S526S|Synonymous_S451S|Silent|Silent|Synonymous_S451S|Silent|Synonymous_S481S|Silent|Synonymous_S368S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.