Variant (rsID / SNP)

rs34813662

rs34813662 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABAT. Location: chromosome 16, position 8,829,626. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ABATBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:8829626
Cytoband: 16p13.2
HGVS: NM_020686.6(ABAT):c.30G>A (p.Leu10=)
Allele change: Synonymous_L10L

Associated conditions / phenotypes

Gamma-aminobutyric acid transaminase deficiency

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.