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rs193922275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs193922275(-;-)
Make rs193922275(-;GC)
ReferenceGRCh38 38.1/141
Chromosome7
Position44145250
GeneGCK
is asnp
is mentioned by
dbSNPrs193922275
ebirs193922275
HLIrs193922275
Exacrs193922275
Varsomers193922275
Maprs193922275
PheGenIrs193922275
hapmaprs193922275
1000 genomesrs193922275
hgdprs193922275
ensemblrs193922275
gopubmedrs193922275
geneviewrs193922275
scholarrs193922275
googlers193922275
pharmgkbrs193922275
gwascentralrs193922275
openSNPrs193922275
23andMers193922275
23andMe allrs193922275
SNP Nexus

SNPshotrs193922275
SNPdbers193922275
MSV3drs193922275
GWAS Ctlgrs193922275
Max Magnitude0
ClinVar
Risk rs193922275(;)
Alt rs193922275(;)
Reference rs193922275(GC;GC)
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.44184849_44184850delGC
CLNSRC ClinVar LabCorp
CLNACC RCV000029854.1,