Variant (rsID / SNP)
rs2274217
rs2274217 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLRX3. Location: chromosome 10, position 131,959,150. The table records no clinical significance for this variant.
Reference-table entries
GLRX3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:131959150
- HGVS
- NM_001199868.2,c.367C>T,p.Pro123Ser
- Allele change
- Missense_P123S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.