Variant (rsID / SNP)

rs13266634

rs13266634 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC30A8. Location: chromosome 8, position 118,184,783. Clinical significance in the table: risk factor.

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Reference-table entries

SLC30A8Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 8:118184783
Cytoband: 8q24.11
HGVS: NM_173851.3(SLC30A8):c.973C>T (p.Arg325Trp)
Allele change: Missense_R276W

Associated conditions / phenotypes

Diabetes mellitus type 2, susceptibility to

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.