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rs193922340

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922340(G;T)
Make rs193922340(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44146530
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs193922340
dbSNP (classic)rs193922340
ClinGenrs193922340
ebirs193922340
HLIrs193922340
Exacrs193922340
Gnomadrs193922340
Varsomers193922340
LitVarrs193922340
Maprs193922340
PheGenIrs193922340
Biobankrs193922340
1000 genomesrs193922340
hgdprs193922340
ensemblrs193922340
geneviewrs193922340
scholarrs193922340
googlers193922340
pharmgkbrs193922340
gwascentralrs193922340
openSNPrs193922340
23andMers193922340
SNPshotrs193922340
SNPdbers193922340
MSV3drs193922340
GWAS Ctlgrs193922340
Max Magnitude0
ClinVar
Risk rs193922340(T;T)
Alt rs193922340(T;T)
Reference Rs193922340(G;G)
Significance Probable-Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene GCK
CLNDBN Maturity-onset diabetes of the young, type 2
Reversed 1
HGVS NC_000007.13:g.44186129C>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029931.1,