Variant (rsID / SNP)

rs76752438

rs76752438 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PNKD. Location: chromosome 2, position 219,210,897. Clinical significance in the table: Benign.

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Reference-table entries

PNKDBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:219210897
Cytoband: 2q35
HGVS: NM_015488.5(PNKD):c.*1193C>T
Allele change: Silent

Associated conditions / phenotypes

Paroxysmal nonkinesigenic dyskinesia 1

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.