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rs1057521092

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521092(A;A)
Make rs1057521092(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44145651
GeneGCK
is asnp
is mentioned by
dbSNPrs1057521092
dbSNP (old)rs1057521092
ClinGenrs1057521092
ebirs1057521092
HLIrs1057521092
Exacrs1057521092
Gnomadrs1057521092
Varsomers1057521092
Maprs1057521092
PheGenIrs1057521092
Biobankrs1057521092
1000 genomesrs1057521092
hgdprs1057521092
ensemblrs1057521092
gopubmedrs1057521092
geneviewrs1057521092
scholarrs1057521092
googlers1057521092
pharmgkbrs1057521092
gwascentralrs1057521092
openSNPrs1057521092
23andMers1057521092
23andMe allrs1057521092
SNPshotrs1057521092
SNPdbers1057521092
MSV3drs1057521092
GWAS Ctlgrs1057521092
Max Magnitude0
ClinVar
Risk rs1057521092(A;A)
Alt rs1057521092(A;A)
Reference Rs1057521092(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44185250C>T
CLNSRC
CLNACC RCV000440624.1,