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

rs193922301

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922301(A;G)
Make rs193922301(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44150976
GeneGCK
is asnp
is mentioned by
dbSNPrs193922301
ebirs193922301
HLIrs193922301
Exacrs193922301
Varsomers193922301
Maprs193922301
PheGenIrs193922301
hapmaprs193922301
1000 genomesrs193922301
hgdprs193922301
ensemblrs193922301
gopubmedrs193922301
geneviewrs193922301
scholarrs193922301
googlers193922301
pharmgkbrs193922301
gwascentralrs193922301
openSNPrs193922301
23andMers193922301
23andMe allrs193922301
SNP Nexus

SNPshotrs193922301
SNPdbers193922301
MSV3drs193922301
GWAS Ctlgrs193922301
Max Magnitude0
ClinVar
Risk rs193922301(G;G)
Alt rs193922301(G;G)
Reference rs193922301(A;A)
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.44190575T>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029886.1,