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rs863224022

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224022(A;A)
Make rs863224022(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position42911317
GeneG6PC
is asnp
is mentioned by
dbSNPrs863224022
ebirs863224022
HLIrs863224022
Exacrs863224022
Varsomers863224022
Maprs863224022
PheGenIrs863224022
hapmaprs863224022
1000 genomesrs863224022
hgdprs863224022
ensemblrs863224022
gopubmedrs863224022
geneviewrs863224022
scholarrs863224022
googlers863224022
pharmgkbrs863224022
gwascentralrs863224022
openSNPrs863224022
23andMers863224022
23andMe allrs863224022
SNP Nexus

SNPshotrs863224022
SNPdbers863224022
MSV3drs863224022
GWAS Ctlgrs863224022
Max Magnitude0
ClinVar
Risk rs863224022(A;A)
Alt rs863224022(A;A)
Reference rs863224022(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene G6PC
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.41063334T>A
CLNSRC
CLNACC RCV000200377.1,