Variant (rsID / SNP)

rs111294347

rs111294347 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLMAP. Location: chromosome 3, position 57,857,439. Clinical significance in the table: Benign.

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Reference-table entries

SLMAPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:57857439
Cytoband: 3p14.3
HGVS: NM_001377540.1(SLMAP):c.1300+14A>G
Allele change: Silent

Associated conditions / phenotypes

Brugada syndrome

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.