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rs587776757

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776757(A;G)
Make rs587776757(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position42901110
GeneG6PC
is asnp
is mentioned by
dbSNPrs587776757
ebirs587776757
HLIrs587776757
Exacrs587776757
Varsomers587776757
Maprs587776757
PheGenIrs587776757
hapmaprs587776757
1000 genomesrs587776757
hgdprs587776757
ensemblrs587776757
gopubmedrs587776757
geneviewrs587776757
scholarrs587776757
googlers587776757
pharmgkbrs587776757
gwascentralrs587776757
openSNPrs587776757
23andMers587776757
23andMe allrs587776757
SNP Nexus

SNPshotrs587776757
SNPdbers587776757
MSV3drs587776757
GWAS Ctlgrs587776757
Max Magnitude0
ClinVar
Risk rs587776757(G;G)
Alt rs587776757(G;G)
Reference rs587776757(A;A)
Significance Pathogenic
Disease Glycogen storage disease type 1A
Variation info
Gene G6PC
CLNDBN Glycogen storage disease type 1A
Reversed 0
HGVS NC_000017.10:g.41053127A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012782.3,