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rs786204740

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786204740(A;G)
Make rs786204740(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position119029369
GeneSLC37A4
is asnp
is mentioned by
dbSNPrs786204740
ebirs786204740
HLIrs786204740
Exacrs786204740
Varsomers786204740
Maprs786204740
PheGenIrs786204740
hapmaprs786204740
1000 genomesrs786204740
hgdprs786204740
ensemblrs786204740
gopubmedrs786204740
geneviewrs786204740
scholarrs786204740
googlers786204740
pharmgkbrs786204740
gwascentralrs786204740
openSNPrs786204740
23andMers786204740
23andMe allrs786204740
SNP Nexus

SNPshotrs786204740
SNPdbers786204740
MSV3drs786204740
GWAS Ctlgrs786204740
Max Magnitude0
ClinVar
Risk rs786204740(G;G)
Alt rs786204740(G;G)
Reference rs786204740(A;A)
Significance Probable-Pathogenic
Disease Glucose-6-phosphate transport defect
Variation info
Gene SLC37A4
CLNDBN Glucose-6-phosphate transport defect
Reversed 1
HGVS NC_000011.9:g.118900079T>C
CLNSRC
CLNACC RCV000169589.1,