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rs193922309

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922309(A;G)
Make rs193922309(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149852
GeneGCK
is asnp
is mentioned by
dbSNPrs193922309
ebirs193922309
HLIrs193922309
Exacrs193922309
Varsomers193922309
Maprs193922309
PheGenIrs193922309
hapmaprs193922309
1000 genomesrs193922309
hgdprs193922309
ensemblrs193922309
gopubmedrs193922309
geneviewrs193922309
scholarrs193922309
googlers193922309
pharmgkbrs193922309
gwascentralrs193922309
openSNPrs193922309
23andMers193922309
23andMe allrs193922309
SNP Nexus

SNPshotrs193922309
SNPdbers193922309
MSV3drs193922309
GWAS Ctlgrs193922309
Max Magnitude0
ClinVar
Risk rs193922309(G;G)
Alt rs193922309(G;G)
Reference rs193922309(A;A)
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.44189451T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029894.1,