Variant (rsID / SNP)

rs113941736

rs113941736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP41. Location: chromosome 7, position 130,040,587. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CEP41Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:130040587
Cytoband: 7q32.2
HGVS: NM_018718.3(CEP41):c.718T>G (p.Cys240Gly)
Allele change: Missense_C240G

Associated conditions / phenotypes

Joubert syndrome 15

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.