Variant (rsID / SNP)

rs137852874

rs137852874 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCKDHA. Location: chromosome 19, position 41,928,167. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

BCKDHALikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 19:41928167
Cytoband: 19q13.2
HGVS: NM_000709.4(BCKDHA):c.745G>A (p.Gly249Ser)
Allele change: Missense_G249S

Associated conditions / phenotypes

Maple syrup urine disease type 1A|Maple syrup urine disease

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.