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rs786204637

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204637(A;A)
Make rs786204637(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position119028193
GeneSLC37A4
is asnp
is mentioned by
dbSNPrs786204637
ebirs786204637
HLIrs786204637
Exacrs786204637
Varsomers786204637
Maprs786204637
PheGenIrs786204637
hapmaprs786204637
1000 genomesrs786204637
hgdprs786204637
ensemblrs786204637
gopubmedrs786204637
geneviewrs786204637
scholarrs786204637
googlers786204637
pharmgkbrs786204637
gwascentralrs786204637
openSNPrs786204637
23andMers786204637
23andMe allrs786204637
SNP Nexus

SNPshotrs786204637
SNPdbers786204637
MSV3drs786204637
GWAS Ctlgrs786204637
Max Magnitude0
ClinVar
Risk rs786204637(A;A)
Alt rs786204637(A;A)
Reference rs786204637(G;G)
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.118898903C>T
CLNSRC
CLNACC RCV000169418.1,