Variant (rsID / SNP)

rs193922311

rs193922311 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCK. Location: chromosome 7, position 44,189,433. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GCKConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 7:44189433
Cytoband: 7p13
HGVS: NM_000162.5(GCK):c.605T>C (p.Met202Thr)
Allele change: Missense_M202T

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.