Variant (rsID / SNP)

rs4402960

rs4402960 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGF2BP2. Location: chromosome 3, position 185,511,687. Clinical significance in the table: risk factor.

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Reference-table entries

IGF2BP2Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 3:185511687
Cytoband: 3q27.2
HGVS: NM_006548.6(IGF2BP2):c.239+29254C>A
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.