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rs863224023

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224023(C;C)
Make rs863224023(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position42901107
GeneG6PC
is asnp
is mentioned by
dbSNPrs863224023
ebirs863224023
HLIrs863224023
Exacrs863224023
Varsomers863224023
Maprs863224023
PheGenIrs863224023
hapmaprs863224023
1000 genomesrs863224023
hgdprs863224023
ensemblrs863224023
gopubmedrs863224023
geneviewrs863224023
scholarrs863224023
googlers863224023
pharmgkbrs863224023
gwascentralrs863224023
openSNPrs863224023
23andMers863224023
23andMe allrs863224023
SNP Nexus

SNPshotrs863224023
SNPdbers863224023
MSV3drs863224023
GWAS Ctlgrs863224023
Max Magnitude0
ClinVar
Risk rs863224023(C;C)
Alt rs863224023(C;C)
Reference rs863224023(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene G6PC
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.41053124G>C
CLNSRC
CLNACC RCV000195822.1,