Variant (rsID / SNP)

rs59191035

rs59191035 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDYN. Location: chromosome 20, position 1,963,610. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PDYNBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 20:1963610
Cytoband: 20p13
HGVS: NM_024411.5(PDYN):c.121A>G (p.Asn41Asp)
Allele change: Silent

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.