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rs1064794268

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome7
Position44153396
GeneGCK
is asnp
is mentioned by
dbSNPrs1064794268
dbSNP (old)rs1064794268
ClinGenrs1064794268
ebirs1064794268
HLIrs1064794268
Exacrs1064794268
Gnomadrs1064794268
Varsomers1064794268
Maprs1064794268
PheGenIrs1064794268
Biobankrs1064794268
1000 genomesrs1064794268
hgdprs1064794268
ensemblrs1064794268
gopubmedrs1064794268
geneviewrs1064794268
scholarrs1064794268
googlers1064794268
pharmgkbrs1064794268
gwascentralrs1064794268
openSNPrs1064794268
23andMers1064794268
23andMe allrs1064794268
SNPshotrs1064794268
SNPdbers1064794268
MSV3drs1064794268
GWAS Ctlgrs1064794268
Max Magnitude0
ClinVar
Risk rs1064794268(C;C)
Alt rs1064794268(C;C)
Reference Rs1064794268(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44192995T>G
CLNSRC
CLNACC RCV000480480.1,