Variant (rsID / SNP)

rs3792267

rs3792267 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAPN10. Location: chromosome 2, position 241,531,174. Clinical significance in the table: risk factor.

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Reference-table entries

CAPN10Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 2:241531174
Cytoband: 2q37.3
HGVS: NM_023083.4(CAPN10):c.471-176G>A
Allele change: Silent

Associated conditions / phenotypes

Type 2 diabetes mellitus 1, 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.