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rs387907313

From SNPedia

Orientationminus
Stabilizedminus
Make rs387907313(C;C)
Make rs387907313(C;T)
Make rs387907313(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position42929766
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs387907313
dbSNP (old)rs387907313
ClinGenrs387907313
ebirs387907313
HLIrs387907313
Exacrs387907313
Varsomers387907313
Maprs387907313
PheGenIrs387907313
Biobankrs387907313
1000 genomesrs387907313
hgdprs387907313
ensemblrs387907313
gopubmedrs387907313
geneviewrs387907313
scholarrs387907313
googlers387907313
pharmgkbrs387907313
gwascentralrs387907313
openSNPrs387907313
23andMers387907313
23andMe allrs387907313
SNP Nexus

SNPshotrs387907313
SNPdbers387907313
MSV3drs387907313
GWAS Ctlgrs387907313
Max Magnitude
ClinVar
Risk rs387907313(T;T)
Alt rs387907313(T;T)
Reference rs387907313(C;C)
Significance Other
Disease Epilepsy not provided
Variation info
Gene SLC2A1
CLNDBN Epilepsy, idiopathic generalized, susceptibility to, 12 not provided
Reversed 1
HGVS NC_000001.10:g.43395437G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000030841.2, RCV000189356.1,