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rs193922314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCT;CCT) 0 common in clinvar
Make rs193922314(-;-)
Make rs193922314(-;CCT)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149802
GeneGCK
is asnp
is mentioned by
dbSNPrs193922314
ebirs193922314
HLIrs193922314
Exacrs193922314
Varsomers193922314
Maprs193922314
PheGenIrs193922314
hapmaprs193922314
1000 genomesrs193922314
hgdprs193922314
ensemblrs193922314
gopubmedrs193922314
geneviewrs193922314
scholarrs193922314
googlers193922314
pharmgkbrs193922314
gwascentralrs193922314
openSNPrs193922314
23andMers193922314
23andMe allrs193922314
SNP Nexus

SNPshotrs193922314
SNPdbers193922314
MSV3drs193922314
GWAS Ctlgrs193922314
Max Magnitude0
ClinVar
Risk rs193922314(;)
Alt rs193922314(;)
Reference rs193922314(CCT;CCT)
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.44189401_44189403delAGG
CLNSRC ClinVar
CLNACC RCV000029900.1,