Variant (rsID / SNP)

rs13342232

rs13342232 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC16A11. Location: chromosome 17, position 6,945,940. The table records no clinical significance for this variant.

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Reference-table entries

SLC16A11Not classified

Variant type: synonymous_variant
Chromosome / position: 17:6945940
HGVS: NM_001370549.1,c.489T>C,p.Leu163Leu
Allele change: Synonymous_L187L

Associated conditions / phenotypes

Gestational Diabetes|Diabetes Mellitus

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.