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rs193922265

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922265(A;A)
Make rs193922265(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145614
GeneGCK
is asnp
is mentioned by
dbSNPrs193922265
ebirs193922265
HLIrs193922265
Exacrs193922265
Varsomers193922265
Maprs193922265
PheGenIrs193922265
hapmaprs193922265
1000 genomesrs193922265
hgdprs193922265
ensemblrs193922265
gopubmedrs193922265
geneviewrs193922265
scholarrs193922265
googlers193922265
pharmgkbrs193922265
gwascentralrs193922265
openSNPrs193922265
23andMers193922265
23andMe allrs193922265
SNP Nexus

SNPshotrs193922265
SNPdbers193922265
MSV3drs193922265
GWAS Ctlgrs193922265
Max Magnitude0
ClinVar
Risk rs193922265(A;A)
Alt rs193922265(A;A)
Reference rs193922265(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.44185213G>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029840.1,