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rs1057520109

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520109(G;T)
Make rs1057520109(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position44153338
GeneGCK
is asnp
is mentioned by
dbSNPrs1057520109
dbSNP (classic)rs1057520109
ClinGenrs1057520109
ebirs1057520109
HLIrs1057520109
Exacrs1057520109
Gnomadrs1057520109
Varsomers1057520109
LitVarrs1057520109
Maprs1057520109
PheGenIrs1057520109
Biobankrs1057520109
1000 genomesrs1057520109
hgdprs1057520109
ensemblrs1057520109
geneviewrs1057520109
scholarrs1057520109
googlers1057520109
pharmgkbrs1057520109
gwascentralrs1057520109
openSNPrs1057520109
23andMers1057520109
23andMe allrs1057520109
SNPshotrs1057520109
SNPdbers1057520109
MSV3drs1057520109
GWAS Ctlgrs1057520109
Max Magnitude0
ClinVar
Risk rs1057520109(A;A) rs1057520109(T;T)
Alt rs1057520109(A;A) rs1057520109(T;T)
Reference Rs1057520109(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GCK
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.44192937C>A; NC_000007.13:g.44192937C>T
CLNSRC
CLNACC RCV000431394.1, RCV000479407.1,