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rs1085307455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position44149977
GeneGCK, LOC105375258
is asnp
is mentioned by
dbSNPrs1085307455
dbSNP (old)rs1085307455
ClinGenrs1085307455
ebirs1085307455
HLIrs1085307455
Exacrs1085307455
Gnomadrs1085307455
Varsomers1085307455
LitVarrs1085307455
Maprs1085307455
PheGenIrs1085307455
Biobankrs1085307455
1000 genomesrs1085307455
hgdprs1085307455
ensemblrs1085307455
gopubmedrs1085307455
geneviewrs1085307455
scholarrs1085307455
googlers1085307455
pharmgkbrs1085307455
gwascentralrs1085307455
openSNPrs1085307455
23andMers1085307455
23andMe allrs1085307455
SNPshotrs1085307455
SNPdbers1085307455
MSV3drs1085307455
GWAS Ctlgrs1085307455
Max Magnitude0
ClinVar
Risk rs1085307455(T;T)
Alt rs1085307455(T;T)
Reference Rs1085307455(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44189576G>A
CLNSRC
CLNACC RCV000490143.1,