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rs193922312

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922312(C;G)
Make rs193922312(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149824
GeneGCK
is asnp
is mentioned by
dbSNPrs193922312
ebirs193922312
HLIrs193922312
Exacrs193922312
Varsomers193922312
Maprs193922312
PheGenIrs193922312
hapmaprs193922312
1000 genomesrs193922312
hgdprs193922312
ensemblrs193922312
gopubmedrs193922312
geneviewrs193922312
scholarrs193922312
googlers193922312
pharmgkbrs193922312
gwascentralrs193922312
openSNPrs193922312
23andMers193922312
23andMe allrs193922312
SNP Nexus

SNPshotrs193922312
SNPdbers193922312
MSV3drs193922312
GWAS Ctlgrs193922312
Max Magnitude0
ClinVar
Risk rs193922312(G;G)
Alt rs193922312(G;G)
Reference rs193922312(C;C)
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.44189423G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029897.1,