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rs193922255

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922255(A;G)
Make rs193922255(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44146464
GeneGCK
is asnp
is mentioned by
dbSNPrs193922255
ebirs193922255
HLIrs193922255
Exacrs193922255
Varsomers193922255
Maprs193922255
PheGenIrs193922255
hapmaprs193922255
1000 genomesrs193922255
hgdprs193922255
ensemblrs193922255
gopubmedrs193922255
geneviewrs193922255
scholarrs193922255
googlers193922255
pharmgkbrs193922255
gwascentralrs193922255
openSNPrs193922255
23andMers193922255
23andMe allrs193922255
SNP Nexus

SNPshotrs193922255
SNPdbers193922255
MSV3drs193922255
GWAS Ctlgrs193922255
Max Magnitude0
ClinVar
Risk rs193922255(G;G)
Alt rs193922255(G;G)
Reference rs193922255(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.44186063T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029830.1,