Variant (rsID / SNP)
rs4959788
rs4959788 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSMG4. Location: chromosome 6, position 3,264,526. The table records no clinical significance for this variant.
Reference-table entries
PSMG4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:3264526
- HGVS
- NM_001128592.2,c.334C>T,p.Leu112Phe
- Allele change
- Missense_L112F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.