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rs794727236

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727236(A;A)
Make rs794727236(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position44153391
GeneGCK
is asnp
is mentioned by
dbSNPrs794727236
ebirs794727236
HLIrs794727236
Exacrs794727236
Varsomers794727236
Maprs794727236
PheGenIrs794727236
hapmaprs794727236
1000 genomesrs794727236
hgdprs794727236
ensemblrs794727236
gopubmedrs794727236
geneviewrs794727236
scholarrs794727236
googlers794727236
pharmgkbrs794727236
gwascentralrs794727236
openSNPrs794727236
23andMers794727236
23andMe allrs794727236
SNP Nexus

SNPshotrs794727236
SNPdbers794727236
MSV3drs794727236
GWAS Ctlgrs794727236
Max Magnitude0
ClinVar
Risk rs794727236(A;A)
Alt rs794727236(A;A)
Reference rs794727236(G;G)
Significance Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene GCK
CLNDBN Maturity-onset diabetes of the young, type 2
Reversed 1
HGVS NC_000007.13:g.44192990C>T
CLNSRC
CLNACC RCV000175536.1,