Variant (rsID / SNP)

rs4608967

rs4608967 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GABRA1. Location: chromosome 5, position 161,275,413. Clinical significance in the table: Benign.

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Reference-table entries

GABRA1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:161275413
Cytoband: 5q34
HGVS: NM_001127644.2(GABRA1):c.-31C>T
Allele change: Silent

Associated conditions / phenotypes

Epilepsy, idiopathic generalized, susceptibility to, 13

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.