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rs1057524900

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524900(A;A)
Make rs1057524900(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44145173
GeneGCK
is asnp
is mentioned by
dbSNPrs1057524900
dbSNP (old)rs1057524900
ClinGenrs1057524900
ebirs1057524900
HLIrs1057524900
Exacrs1057524900
Gnomadrs1057524900
Varsomers1057524900
Maprs1057524900
PheGenIrs1057524900
Biobankrs1057524900
1000 genomesrs1057524900
hgdprs1057524900
ensemblrs1057524900
gopubmedrs1057524900
geneviewrs1057524900
scholarrs1057524900
googlers1057524900
pharmgkbrs1057524900
gwascentralrs1057524900
openSNPrs1057524900
23andMers1057524900
23andMe allrs1057524900
SNPshotrs1057524900
SNPdbers1057524900
MSV3drs1057524900
GWAS Ctlgrs1057524900
Max Magnitude0
ClinVar
Risk rs1057524900(A;A)
Alt rs1057524900(A;A)
Reference Rs1057524900(C;C)
Significance Probable-Pathogenic
Disease Monogenic diabetes
Variation info
Gene GCK
CLNDBN Monogenic diabetes
Reversed 1
HGVS NC_000007.13:g.44184772G>T
CLNSRC
CLNACC RCV000445420.1,