Variant (rsID / SNP)

rs3751582

rs3751582 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GABRB3. Location: chromosome 15, position 26,806,064. Clinical significance in the table: Benign.

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Reference-table entries

GABRB3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:26806064
Cytoband: 15q12
HGVS: NM_000814.6(GABRB3):c.1080+15A>G
Allele change: Silent

Associated conditions / phenotypes

Developmental and epileptic encephalopathy, 43|Epilepsy, childhood absence, susceptibility to, 1|Epilepsy, childhood absence, susceptibility to, 5

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.