Variant (rsID / SNP)

rs193922336

rs193922336 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCK. Location: chromosome 7, position 44,186,174. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

GCKLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 7:44186174
Cytoband: 7p13
HGVS: NM_000162.5(GCK):c.907C>T (p.Arg303Trp)
Allele change: Missense_R303W

Associated conditions / phenotypes

Maturity-onset diabetes of the young type 2

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.