Have questions? Visit https://www.reddit.com/r/SNPedia

rs193921340

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193921340(A;A)
Make rs193921340(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145581
GeneGCK
is asnp
is mentioned by
dbSNPrs193921340
ebirs193921340
HLIrs193921340
Exacrs193921340
Varsomers193921340
Maprs193921340
PheGenIrs193921340
hapmaprs193921340
1000 genomesrs193921340
hgdprs193921340
ensemblrs193921340
gopubmedrs193921340
geneviewrs193921340
scholarrs193921340
googlers193921340
pharmgkbrs193921340
gwascentralrs193921340
openSNPrs193921340
23andMers193921340
23andMe allrs193921340
SNP Nexus

SNPshotrs193921340
SNPdbers193921340
MSV3drs193921340
GWAS Ctlgrs193921340
Max Magnitude0
ClinVar
Risk rs193921340(A,C;A,C)
Alt rs193921340(A,C;A,C)
Reference rs193921340(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.44185180A>G; NC_000007.13:g.44185180A>T
CLNSRC ClinVar LabCorp
CLNACC RCV000029847.1, RCV000029846.1,