Variant (rsID / SNP)

rs7172

rs7172 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSMB4. Location: chromosome 1, position 151,372,138. The table records no clinical significance for this variant.

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Reference-table entries

PSMB4Not classified

Variant type: synonymous_variant
Chromosome / position: 1:151372138
HGVS: NM_002796.3,c.75G>A,p.Pro25Pro
Allele change: Synonymous_P25P

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.