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rs193922330

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922330(C;C)
Make rs193922330(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44147734
GeneGCK
is asnp
is mentioned by
dbSNPrs193922330
ebirs193922330
HLIrs193922330
Exacrs193922330
Varsomers193922330
Maprs193922330
PheGenIrs193922330
hapmaprs193922330
1000 genomesrs193922330
hgdprs193922330
ensemblrs193922330
gopubmedrs193922330
geneviewrs193922330
scholarrs193922330
googlers193922330
pharmgkbrs193922330
gwascentralrs193922330
openSNPrs193922330
23andMers193922330
23andMe allrs193922330
SNP Nexus

SNPshotrs193922330
SNPdbers193922330
MSV3drs193922330
GWAS Ctlgrs193922330
Max Magnitude0
ClinVar
Risk rs193922330(C;C)
Alt rs193922330(C;C)
Reference rs193922330(T;T)
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.44187333A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029920.1,