Variant (rsID / SNP)

rs367543061

rs367543061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPLANE1. Location: chromosome 5, position 37,187,590. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

CPLANE1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 5:37187590
Cytoband: 5p13.2
HGVS: NM_001384732.1(CPLANE1):c.4006C>T (p.Arg1336Trp)
Allele change: Missense_R1336W

Associated conditions / phenotypes

Joubert syndrome 17|Joubert syndrome and related disorders

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.