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rs193922305

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922305(A;A)
Make rs193922305(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44150016
GeneGCK
is asnp
is mentioned by
dbSNPrs193922305
ebirs193922305
HLIrs193922305
Exacrs193922305
Varsomers193922305
Maprs193922305
PheGenIrs193922305
hapmaprs193922305
1000 genomesrs193922305
hgdprs193922305
ensemblrs193922305
gopubmedrs193922305
geneviewrs193922305
scholarrs193922305
googlers193922305
pharmgkbrs193922305
gwascentralrs193922305
openSNPrs193922305
23andMers193922305
23andMe allrs193922305
SNP Nexus

SNPshotrs193922305
SNPdbers193922305
MSV3drs193922305
GWAS Ctlgrs193922305
Max Magnitude0
ClinVar
Risk rs193922305(A;A)
Alt rs193922305(A;A)
Reference rs193922305(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.44189615C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029890.1,