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rs1057524901

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524901(-;-)
Make rs1057524901(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44145190
GeneGCK
is asnp
is mentioned by
dbSNPrs1057524901
dbSNP (old)rs1057524901
ClinGenrs1057524901
ebirs1057524901
HLIrs1057524901
Exacrs1057524901
Gnomadrs1057524901
Varsomers1057524901
Maprs1057524901
PheGenIrs1057524901
Biobankrs1057524901
1000 genomesrs1057524901
hgdprs1057524901
ensemblrs1057524901
gopubmedrs1057524901
geneviewrs1057524901
scholarrs1057524901
googlers1057524901
pharmgkbrs1057524901
gwascentralrs1057524901
openSNPrs1057524901
23andMers1057524901
23andMe allrs1057524901
SNPshotrs1057524901
SNPdbers1057524901
MSV3drs1057524901
GWAS Ctlgrs1057524901
Max Magnitude0
ClinVar
Risk rs1057524901(-;-)
Alt rs1057524901(-;-)
Reference Rs1057524901(C;C)
Significance Probable-Pathogenic
Disease Monogenic diabetes
Variation info
Gene GCK
CLNDBN Monogenic diabetes
Reversed 1
HGVS NC_000007.13:g.44184789delG
CLNSRC
CLNACC RCV000445487.1,