Variant (rsID / SNP)

rs11541756

rs11541756 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSMD8. Location: chromosome 19, position 38,871,622. The table records no clinical significance for this variant.

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Reference-table entries

PSMD8Not classified

Variant type: synonymous_variant
Chromosome / position: 19:38871622
HGVS: NM_002812.5,c.786C>T,p.Ile262Ile
Allele change: Synonymous_I262I

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.