Variant (rsID / SNP)

rs1266889

rs1266889 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKHD1. Location: chromosome 6, position 51,799,166. Clinical significance in the table: Benign.

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Reference-table entries

PKHD1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:51799166
Cytoband: 6p12.2
HGVS: NM_138694.4(PKHD1):c.5909-46A>G
Allele change: Silent

Associated conditions / phenotypes

Polycystic kidney disease 4|Autosomal recessive polycystic kidney disease

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.