Variant (rsID / SNP)

rs10946398

rs10946398 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDKAL1. Location: chromosome 6, position 20,661,034. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CDKAL1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:20661034
Cytoband: 6p22.3
HGVS: NM_017774.3(CDKAL1):c.371+11426A>C
Allele change: Silent

Associated conditions / phenotypes

Type 2 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.