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rs80359841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80359841(A;A)
Make rs80359841(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position42958633
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs80359841
ebirs80359841
HLIrs80359841
Exacrs80359841
Varsomers80359841
Maprs80359841
PheGenIrs80359841
hapmaprs80359841
1000 genomesrs80359841
hgdprs80359841
ensemblrs80359841
gopubmedrs80359841
geneviewrs80359841
scholarrs80359841
googlers80359841
pharmgkbrs80359841
gwascentralrs80359841
openSNPrs80359841
23andMers80359841
23andMe allrs80359841
SNP Nexus

SNPshotrs80359841
SNPdbers80359841
MSV3drs80359841
GWAS Ctlgrs80359841
Max Magnitude0
ClinVar
Risk rs80359841(A;A)
Alt rs80359841(A;A)
Reference rs80359841(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1-AS1 SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43424304C>T
CLNSRC
CLNACC RCV000189346.2,


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