Variant (rsID / SNP)

rs12255372

rs12255372 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TCF7L2. Location: chromosome 10, position 114,808,902. Clinical significance in the table: risk factor.

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Reference-table entries

TCF7L2Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 10:114808902
Cytoband: 10q25.2
HGVS: NM_001367943.1(TCF7L2):c.552+9017G>T
Allele change: Silent

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.