Variant (rsID / SNP)

rs191333060

rs191333060 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDH19. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PCDH19Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xq22.1
HGVS: NM_001184880.2(PCDH19):c.3319C>G (p.Arg1107Gly)
Allele change: Missense_R1059G

Associated conditions / phenotypes

Developmental and epileptic encephalopathy, 9|Childhood epilepsy with centrotemporal spikes|History of neurodevelopmental disorder

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.