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rs193922319

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922319(C;C)
Make rs193922319(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149762
GeneGCK
is asnp
is mentioned by
dbSNPrs193922319
ebirs193922319
HLIrs193922319
Exacrs193922319
Varsomers193922319
Maprs193922319
PheGenIrs193922319
hapmaprs193922319
1000 genomesrs193922319
hgdprs193922319
ensemblrs193922319
gopubmedrs193922319
geneviewrs193922319
scholarrs193922319
googlers193922319
pharmgkbrs193922319
gwascentralrs193922319
openSNPrs193922319
23andMers193922319
23andMe allrs193922319
SNP Nexus

SNPshotrs193922319
SNPdbers193922319
MSV3drs193922319
GWAS Ctlgrs193922319
Max Magnitude0
ClinVar
Risk rs193922319(C;C)
Alt rs193922319(C;C)
Reference rs193922319(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.44189361A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029907.1,