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Variant (rsID / SNP)

rs648396

PERP

rs648396 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PERP. Location: chromosome 6, position 138,413,269. The table records no clinical significance for this variant.

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Reference-table entries

PERPNot classified
Variant type
synonymous_variant
Chromosome / position
6:138413269
HGVS
NM_022121.5,c.492T>C,p.Ile164Ile
Allele change
Synonymous_I164I

Public references

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