Variant (rsID / SNP)

rs1260326

rs1260326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCKR. Location: chromosome 2, position 27,730,940. Clinical significance in the table: Benign.

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Reference-table entries

GCKRBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:27730940
Cytoband: 2p23.3
HGVS: NM_001486.4(GCKR):c.1337T>C (p.Leu446Pro)
Allele change: Missense_L446P

Associated conditions / phenotypes

Fasting plasma glucose level quantitative trait locus 5

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.