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rs781784543

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781784543(A;A)
Make rs781784543(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position119026979
GeneSLC37A4
is asnp
is mentioned by
dbSNPrs781784543
ebirs781784543
HLIrs781784543
Exacrs781784543
Varsomers781784543
Maprs781784543
PheGenIrs781784543
hapmaprs781784543
1000 genomesrs781784543
hgdprs781784543
ensemblrs781784543
gopubmedrs781784543
geneviewrs781784543
scholarrs781784543
googlers781784543
pharmgkbrs781784543
gwascentralrs781784543
openSNPrs781784543
23andMers781784543
23andMe allrs781784543
SNP Nexus

SNPshotrs781784543
SNPdbers781784543
MSV3drs781784543
GWAS Ctlgrs781784543
Max Magnitude0
ClinVar
Risk rs781784543(A;A)
Alt rs781784543(A;A)
Reference rs781784543(G;G)
Significance Probable-Pathogenic
Disease Glucose-6-phosphate transport defect
Variation info
Gene SLC37A4
CLNDBN Glucose-6-phosphate transport defect
Reversed 0
HGVS NC_000011.9:g.118897689G>A
CLNSRC
CLNACC RCV000169082.1,