Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057521094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521094(A;A)
Make rs1057521094(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44151076
GeneGCK
is asnp
is mentioned by
dbSNPrs1057521094
dbSNP (classic)rs1057521094
ClinGenrs1057521094
ebirs1057521094
HLIrs1057521094
Exacrs1057521094
Gnomadrs1057521094
Varsomers1057521094
LitVarrs1057521094
Maprs1057521094
PheGenIrs1057521094
Biobankrs1057521094
1000 genomesrs1057521094
hgdprs1057521094
ensemblrs1057521094
geneviewrs1057521094
scholarrs1057521094
googlers1057521094
pharmgkbrs1057521094
gwascentralrs1057521094
openSNPrs1057521094
23andMers1057521094
23andMe allrs1057521094
SNPshotrs1057521094
SNPdbers1057521094
MSV3drs1057521094
GWAS Ctlgrs1057521094
Max Magnitude0
ClinVar
Risk rs1057521094(A;A)
Alt rs1057521094(A;A)
Reference Rs1057521094(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44190675C>T
CLNSRC
CLNACC RCV000429688.1,