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rs1057521093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521093(A;G)
Make rs1057521093(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44147810
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs1057521093
dbSNP (old)rs1057521093
ClinGenrs1057521093
ebirs1057521093
HLIrs1057521093
Exacrs1057521093
Gnomadrs1057521093
Varsomers1057521093
LitVarrs1057521093
Maprs1057521093
PheGenIrs1057521093
Biobankrs1057521093
1000 genomesrs1057521093
hgdprs1057521093
ensemblrs1057521093
gopubmedrs1057521093
geneviewrs1057521093
scholarrs1057521093
googlers1057521093
pharmgkbrs1057521093
gwascentralrs1057521093
openSNPrs1057521093
23andMers1057521093
23andMe allrs1057521093
SNPshotrs1057521093
SNPdbers1057521093
MSV3drs1057521093
GWAS Ctlgrs1057521093
Max Magnitude0
ClinVar
Risk rs1057521093(G;G)
Alt rs1057521093(G;G)
Reference Rs1057521093(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44187409T>C
CLNSRC
CLNACC RCV000419860.1,