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rs1057524906

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524906(C;C)
Make rs1057524906(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44153387
GeneGCK
is asnp
is mentioned by
dbSNPrs1057524906
dbSNP (old)rs1057524906
ClinGenrs1057524906
ebirs1057524906
HLIrs1057524906
Exacrs1057524906
Gnomadrs1057524906
Varsomers1057524906
Maprs1057524906
PheGenIrs1057524906
Biobankrs1057524906
1000 genomesrs1057524906
hgdprs1057524906
ensemblrs1057524906
gopubmedrs1057524906
geneviewrs1057524906
scholarrs1057524906
googlers1057524906
pharmgkbrs1057524906
gwascentralrs1057524906
openSNPrs1057524906
23andMers1057524906
23andMe allrs1057524906
SNPshotrs1057524906
SNPdbers1057524906
MSV3drs1057524906
GWAS Ctlgrs1057524906
Max Magnitude0
ClinVar
Risk rs1057524906(C;C)
Alt rs1057524906(C;C)
Reference Rs1057524906(T;T)
Significance Probable-Pathogenic
Disease Monogenic diabetes
Variation info
Gene GCK
CLNDBN Monogenic diabetes
Reversed 1
HGVS NC_000007.13:g.44192986A>G
CLNSRC
CLNACC RCV000445500.1,