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

rs1057524902

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524902(A;A)
Make rs1057524902(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44145495
GeneGCK
is asnp
is mentioned by
dbSNPrs1057524902
dbSNP (old)rs1057524902
ClinGenrs1057524902
ebirs1057524902
HLIrs1057524902
Exacrs1057524902
Gnomadrs1057524902
Varsomers1057524902
Maprs1057524902
PheGenIrs1057524902
Biobankrs1057524902
1000 genomesrs1057524902
hgdprs1057524902
ensemblrs1057524902
gopubmedrs1057524902
geneviewrs1057524902
scholarrs1057524902
googlers1057524902
pharmgkbrs1057524902
gwascentralrs1057524902
openSNPrs1057524902
23andMers1057524902
23andMe allrs1057524902
SNPshotrs1057524902
SNPdbers1057524902
MSV3drs1057524902
GWAS Ctlgrs1057524902
Max Magnitude0
ClinVar
Risk rs1057524902(A;A)
Alt rs1057524902(A;A)
Reference Rs1057524902(T;T)
Significance Pathogenic
Disease Monogenic diabetes
Variation info
Gene GCK
CLNDBN Monogenic diabetes
Reversed 1
HGVS NC_000007.13:g.44185094A>T
CLNSRC
CLNACC RCV000445532.1,