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Variant (rsID / SNP)

rs146175795

GCKR

rs146175795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCKR. Location: chromosome 2, position 27,721,143. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GCKRConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:27721143
Cytoband
2p23.3
HGVS
NM_001486.4(GCKR):c.307G>A (p.Val103Met)
Allele change
Missense_V103M

Associated conditions / phenotypes

Fasting plasma glucose level quantitative trait locus 5|Hypertriglyceridemia

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.