Variant (rsID / SNP)

rs147477305

rs147477305 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDP1. Location: chromosome 8, position 94,935,718. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PDP1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:94935718
Cytoband: 8q22.1
HGVS: NM_018444.4(PDP1):c.1431C>T (p.Asn477=)
Allele change: Synonymous_N477N

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.