Variant (rsID / SNP)

rs41311139

rs41311139 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DEPDC5. Location: chromosome 22, position 32,200,849. Clinical significance in the table: Benign.

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Reference-table entries

DEPDC5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:32200849
Cytoband: 22q12.3
HGVS: NM_001242896.3(DEPDC5):c.1165C>T (p.Arg389Cys)
Allele change: Missense_R389C

Associated conditions / phenotypes

Familial focal epilepsy with variable foci|Seizure

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.