Variant (rsID / SNP)

rs2302768

rs2302768 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSMG2. Location: chromosome 18, position 12,718,593. The table records no clinical significance for this variant.

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Reference-table entries

PSMG2Not classified

Variant type: synonymous_variant
Chromosome / position: 18:12718593
HGVS: NM_020232.5,c.366A>G,p.Ser122Ser
Allele change: Synonymous_S91S

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.