Variant (rsID / SNP)
rs1065356
rs1065356 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LY6G6C, MPIG6B. Location: chromosome 6, position 31,687,008. The table records no clinical significance for this variant.
Reference-table entries
LY6G6CNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:31687008
- HGVS
- NM_025261.3,c.243C>T,p.Arg81Arg
- Allele change
- Synonymous_R81R
Associated conditions / phenotypes
Kaposi Sarcoma|Sarcoma|Spindle Cell Sarcoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.