Variant (rsID / SNP)

rs146485488

rs146485488 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR62. Location: chromosome 19, position 36,557,245. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

WDR62Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 19:36557245
Cytoband: 19q13.12
HGVS: NM_001083961.2(WDR62):c.477G>A (p.Ala159=)
Allele change: Synonymous_A159A

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.