Variant (rsID / SNP)

rs9429505

rs9429505 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC16A1. Location: chromosome 1, position 113,454,571. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLC16A1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:113454571
Cytoband: 1p13.2
HGVS: NM_003051.4(SLC16A1):c.*1942T>C
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.