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rs193922335

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922335(A;T)
Make rs193922335(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position44146611
GeneGCK
is asnp
is mentioned by
dbSNPrs193922335
ebirs193922335
HLIrs193922335
Exacrs193922335
Varsomers193922335
Maprs193922335
PheGenIrs193922335
hapmaprs193922335
1000 genomesrs193922335
hgdprs193922335
ensemblrs193922335
gopubmedrs193922335
geneviewrs193922335
scholarrs193922335
googlers193922335
pharmgkbrs193922335
gwascentralrs193922335
openSNPrs193922335
23andMers193922335
23andMe allrs193922335
SNP Nexus

SNPshotrs193922335
SNPdbers193922335
MSV3drs193922335
GWAS Ctlgrs193922335
Max Magnitude0
ClinVar
Risk rs193922335(T;T)
Alt rs193922335(T;T)
Reference rs193922335(A;A)
Significance 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.44186210T>A
CLNSRC ClinVar
CLNACC RCV000029926.1,