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rs193922310

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922310(A;G)
Make rs193922310(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149835
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs193922310
dbSNP (classic)rs193922310
ClinGenrs193922310
ebirs193922310
HLIrs193922310
Exacrs193922310
Gnomadrs193922310
Varsomers193922310
LitVarrs193922310
Maprs193922310
PheGenIrs193922310
Biobankrs193922310
1000 genomesrs193922310
hgdprs193922310
ensemblrs193922310
geneviewrs193922310
scholarrs193922310
googlers193922310
pharmgkbrs193922310
gwascentralrs193922310
openSNPrs193922310
23andMers193922310
SNPshotrs193922310
SNPdbers193922310
MSV3drs193922310
GWAS Ctlgrs193922310
Max Magnitude0
ClinVar
Risk rs193922310(G;G)
Alt rs193922310(G;G)
Reference Rs193922310(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.44189434T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029895.1,