Variant (rsID / SNP)

rs11585690

rs11585690 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC16A1. Location: chromosome 1, position 113,456,368. Clinical significance in the table: Likely benign.

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Reference-table entries

SLC16A1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:113456368
Cytoband: 1p13.2
HGVS: NM_003051.4(SLC16A1):c.*145T>G
Allele change: Silent

Associated conditions / phenotypes

Exercise-induced hyperinsulinism

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.