Variant (rsID / SNP)
rs2657879
rs2657879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLS2. Location: chromosome 12, position 56,865,338. The table records no clinical significance for this variant.
Reference-table entries
GLS2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:56865338
- HGVS
- NM_013267.4,c.1742T>C,p.Leu581Pro
- Allele change
- Missense_L316P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.