Variant (rsID / SNP)

rs138488258

rs138488258 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDP1. Location: chromosome 8, position 94,935,193. Clinical significance in the table: Benign.

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Reference-table entries

PDP1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:94935193
Cytoband: 8q22.1
HGVS: NM_018444.4(PDP1):c.906C>T (p.Asp302=)
Allele change: Synonymous_D302D

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.