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rs80359826

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80359826(C;T)
Make rs80359826(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position42929018
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs80359826
ebirs80359826
HLIrs80359826
Exacrs80359826
Varsomers80359826
Maprs80359826
PheGenIrs80359826
hapmaprs80359826
1000 genomesrs80359826
hgdprs80359826
ensemblrs80359826
gopubmedrs80359826
geneviewrs80359826
scholarrs80359826
googlers80359826
pharmgkbrs80359826
gwascentralrs80359826
openSNPrs80359826
23andMers80359826
23andMe allrs80359826
SNP Nexus

SNPshotrs80359826
SNPdbers80359826
MSV3drs80359826
GWAS Ctlgrs80359826
Max Magnitude0
ClinVar
Risk rs80359826(A,T;A,T)
Alt rs80359826(A,T;A,T)
Reference rs80359826(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43394689G>A
CLNSRC
CLNACC RCV000189360.2,


[PMID 15622525] Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.