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rs193922320

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922320(-;-)
Make rs193922320(-;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position44149759
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs193922320
dbSNP (classic)rs193922320
ClinGenrs193922320
ebirs193922320
HLIrs193922320
Exacrs193922320
Gnomadrs193922320
Varsomers193922320
LitVarrs193922320
Maprs193922320
PheGenIrs193922320
Biobankrs193922320
1000 genomesrs193922320
hgdprs193922320
ensemblrs193922320
geneviewrs193922320
scholarrs193922320
googlers193922320
pharmgkbrs193922320
gwascentralrs193922320
openSNPrs193922320
23andMers193922320
SNPshotrs193922320
SNPdbers193922320
MSV3drs193922320
GWAS Ctlgrs193922320
Max Magnitude0
ClinVar
Risk rs193922320(-;-)
Alt rs193922320(-;-)
Reference Rs193922320(G;G)
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.44189358delC
CLNSRC ClinVar
CLNACC RCV000029908.1,