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rs193922262

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922262(G;T)
Make rs193922262(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145636
GeneGCK
is asnp
is mentioned by
dbSNPrs193922262
ebirs193922262
HLIrs193922262
Exacrs193922262
Varsomers193922262
Maprs193922262
PheGenIrs193922262
hapmaprs193922262
1000 genomesrs193922262
hgdprs193922262
ensemblrs193922262
gopubmedrs193922262
geneviewrs193922262
scholarrs193922262
googlers193922262
pharmgkbrs193922262
gwascentralrs193922262
openSNPrs193922262
23andMers193922262
23andMe allrs193922262
SNP Nexus

SNPshotrs193922262
SNPdbers193922262
MSV3drs193922262
GWAS Ctlgrs193922262
Max Magnitude0
ClinVar
Risk rs193922262(T;T)
Alt rs193922262(T;T)
Reference rs193922262(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.44185235C>A
CLNSRC ClinVar
CLNACC RCV000029837.1,