Variant (rsID / SNP)

rs146779637

rs146779637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to G6PC2. Location: chromosome 2, position 169,764,368. Clinical significance in the table: Uncertain significance.

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Reference-table entries

G6PC2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:169764368
Cytoband: 2q31.1
HGVS: NM_021176.3(G6PC2):c.847C>T (p.Arg283Ter)
Allele change: Nonsense_R283X

Associated conditions / phenotypes

Fasting plasma glucose level quantitative trait locus 1

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.