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rs193302900

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193302900(A;A)
Make rs193302900(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position119026640
GeneSLC37A4
is asnp
is mentioned by
dbSNPrs193302900
ebirs193302900
HLIrs193302900
Exacrs193302900
Varsomers193302900
Maprs193302900
PheGenIrs193302900
hapmaprs193302900
1000 genomesrs193302900
hgdprs193302900
ensemblrs193302900
gopubmedrs193302900
geneviewrs193302900
scholarrs193302900
googlers193302900
pharmgkbrs193302900
gwascentralrs193302900
openSNPrs193302900
23andMers193302900
23andMe allrs193302900
SNP Nexus

SNPshotrs193302900
SNPdbers193302900
MSV3drs193302900
GWAS Ctlgrs193302900
Max Magnitude0
ClinVar
Risk rs193302900(A;A)
Alt rs193302900(A;A)
Reference rs193302900(T;T)
Significance Probable-Pathogenic
Disease not provided Glucose-6-phosphate transport defect
Variation info
Gene SLC37A4
CLNDBN not provided Glucose-6-phosphate transport defect
Reversed 1
HGVS NC_000011.9:g.118897350A>T
CLNSRC UniProtKB (variants)
CLNACC RCV000059143.1, RCV000169410.1,