Variant (rsID / SNP)

rs16022

rs16022 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA1A. Location: chromosome 19, position 13,409,696. Clinical significance in the table: Benign.

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Reference-table entries

CACNA1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:13409696
Cytoband: 19p13.13
HGVS: NM_001127222.2(CACNA1A):c.2751G>C (p.Glu917Asp)
Allele change: Missense_E918D

Associated conditions / phenotypes

History of neurodevelopmental disorder|Developmental and epileptic encephalopathy, 42|Episodic ataxia type 2

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.