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rs1064793134

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position44145663
GeneGCK
is asnp
is mentioned by
dbSNPrs1064793134
dbSNP (old)rs1064793134
ClinGenrs1064793134
ebirs1064793134
HLIrs1064793134
Exacrs1064793134
Gnomadrs1064793134
Varsomers1064793134
LitVarrs1064793134
Maprs1064793134
PheGenIrs1064793134
Biobankrs1064793134
1000 genomesrs1064793134
hgdprs1064793134
ensemblrs1064793134
gopubmedrs1064793134
geneviewrs1064793134
scholarrs1064793134
googlers1064793134
pharmgkbrs1064793134
gwascentralrs1064793134
openSNPrs1064793134
23andMers1064793134
23andMe allrs1064793134
SNPshotrs1064793134
SNPdbers1064793134
MSV3drs1064793134
GWAS Ctlgrs1064793134
Max Magnitude0
ClinVar
Risk rs1064793134(A;A)
Alt rs1064793134(A;A)
Reference Rs1064793134(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44185262C>T
CLNSRC
CLNACC RCV000479890.1,