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rs1057524904

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524904(C;T)
Make rs1057524904(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44147765
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs1057524904
dbSNP (old)rs1057524904
ClinGenrs1057524904
ebirs1057524904
HLIrs1057524904
Exacrs1057524904
Gnomadrs1057524904
Varsomers1057524904
Maprs1057524904
PheGenIrs1057524904
Biobankrs1057524904
1000 genomesrs1057524904
hgdprs1057524904
ensemblrs1057524904
gopubmedrs1057524904
geneviewrs1057524904
scholarrs1057524904
googlers1057524904
pharmgkbrs1057524904
gwascentralrs1057524904
openSNPrs1057524904
23andMers1057524904
23andMe allrs1057524904
SNPshotrs1057524904
SNPdbers1057524904
MSV3drs1057524904
GWAS Ctlgrs1057524904
Max Magnitude0
ClinVar
Risk rs1057524904(T;T)
Alt rs1057524904(T;T)
Reference Rs1057524904(C;C)
Significance Probable-Pathogenic
Disease Monogenic diabetes
Variation info
Gene GCK
CLNDBN Monogenic diabetes
Reversed 1
HGVS NC_000007.13:g.44187364G>A
CLNSRC
CLNACC RCV000445484.1,