Variant (rsID / SNP)

rs72546642

rs72546642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPD1L. Location: chromosome 3, position 32,201,083. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GPD1LBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:32201083
Cytoband: 3p22.3
HGVS: NM_015141.4(GPD1L):c.876G>A (p.Glu292=)
Allele change: Synonymous_E292E

Associated conditions / phenotypes

Brugada syndrome|Cardiovascular phenotype

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.