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rs143321486

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs143321486(C;G)
Make rs143321486(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position42911295
GeneG6PC
is asnp
is mentioned by
dbSNPrs143321486
ebirs143321486
HLIrs143321486
Exacrs143321486
Varsomers143321486
Maprs143321486
PheGenIrs143321486
hapmaprs143321486
1000 genomesrs143321486
hgdprs143321486
ensemblrs143321486
gopubmedrs143321486
geneviewrs143321486
scholarrs143321486
googlers143321486
pharmgkbrs143321486
gwascentralrs143321486
openSNPrs143321486
23andMers143321486
23andMe allrs143321486
SNP Nexus

SNPshotrs143321486
SNPdbers143321486
MSV3drs143321486
GWAS Ctlgrs143321486
Max Magnitude0
ClinVar
Risk rs143321486(G;G)
Alt rs143321486(G;G)
Reference rs143321486(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene G6PC
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.41063312C>G
CLNSRC
CLNACC RCV000199189.1,