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

rs1057524903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524903(A;G)
Make rs1057524903(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44146466
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs1057524903
dbSNP (classic)rs1057524903
ClinGenrs1057524903
ebirs1057524903
HLIrs1057524903
Exacrs1057524903
Gnomadrs1057524903
Varsomers1057524903
LitVarrs1057524903
Maprs1057524903
PheGenIrs1057524903
Biobankrs1057524903
1000 genomesrs1057524903
hgdprs1057524903
ensemblrs1057524903
geneviewrs1057524903
scholarrs1057524903
googlers1057524903
pharmgkbrs1057524903
gwascentralrs1057524903
openSNPrs1057524903
23andMers1057524903
SNPshotrs1057524903
SNPdbers1057524903
MSV3drs1057524903
GWAS Ctlgrs1057524903
Max Magnitude0
ClinVar
Risk rs1057524903(G;G)
Alt rs1057524903(G;G)
Reference Rs1057524903(A;A)
Significance Pathogenic
Disease Monogenic diabetes
Variation info
Gene GCK
CLNDBN Monogenic diabetes
Reversed 1
HGVS NC_000007.13:g.44186065T>C
CLNSRC
CLNACC RCV000445412.1,