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rs193922271

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922271(C;G)
Make rs193922271(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145543
GeneGCK
is asnp
is mentioned by
dbSNPrs193922271
ebirs193922271
HLIrs193922271
Exacrs193922271
Varsomers193922271
Maprs193922271
PheGenIrs193922271
hapmaprs193922271
1000 genomesrs193922271
hgdprs193922271
ensemblrs193922271
gopubmedrs193922271
geneviewrs193922271
scholarrs193922271
googlers193922271
pharmgkbrs193922271
gwascentralrs193922271
openSNPrs193922271
23andMers193922271
23andMe allrs193922271
SNP Nexus

SNPshotrs193922271
SNPdbers193922271
MSV3drs193922271
GWAS Ctlgrs193922271
Max Magnitude0
ClinVar
Risk rs193922271(G;G)
Alt rs193922271(G;G)
Reference rs193922271(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.44185142G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029850.1,