Variant (rsID / SNP)

rs2784198

rs2784198 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKHD1. Location: chromosome 6, position 51,480,486. 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: 6:51480486
Cytoband: 6p12.3
HGVS: NM_138694.4(PKHD1):c.*3393C>A
Allele change: Silent

Associated conditions / phenotypes

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.