Variant (rsID / SNP)

rs4574

rs4574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSMB7. Location: chromosome 9, position 127,177,161. The table records no clinical significance for this variant.

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Reference-table entries

PSMB7Not classified

Variant type: missense_variant
Chromosome / position: 9:127177161
HGVS: NM_002799.4,c.116T>C,p.Val39Ala
Allele change: Missense_V39A

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.