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rs1057524905

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524905(A;A)
Make rs1057524905(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44147834
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs1057524905
dbSNP (old)rs1057524905
ClinGenrs1057524905
ebirs1057524905
HLIrs1057524905
Exacrs1057524905
Gnomadrs1057524905
Varsomers1057524905
Maprs1057524905
PheGenIrs1057524905
Biobankrs1057524905
1000 genomesrs1057524905
hgdprs1057524905
ensemblrs1057524905
gopubmedrs1057524905
geneviewrs1057524905
scholarrs1057524905
googlers1057524905
pharmgkbrs1057524905
gwascentralrs1057524905
openSNPrs1057524905
23andMers1057524905
23andMe allrs1057524905
SNPshotrs1057524905
SNPdbers1057524905
MSV3drs1057524905
GWAS Ctlgrs1057524905
Max Magnitude0
ClinVar
Risk rs1057524905(A;A)
Alt rs1057524905(A;A)
Reference Rs1057524905(G;G)
Significance Pathogenic
Disease Monogenic diabetes
Variation info
Gene GCK
CLNDBN Monogenic diabetes
Reversed 1
HGVS NC_000007.13:g.44187433C>T
CLNSRC
CLNACC RCV000445383.1,