rs387907313

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs387907313(C;T)

Make rs387907313(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

42929766

Gene

SLC2A1

is a	snp
is	mentioned by
dbSNP	rs387907313
dbSNP (classic)	rs387907313
ClinGen	rs387907313
ebi	rs387907313
HLI	rs387907313
Exac	rs387907313
Gnomad	rs387907313
Varsome	rs387907313
LitVar	rs387907313
Map	rs387907313
PheGenI	rs387907313
Biobank	rs387907313
1000 genomes	rs387907313
hgdp	rs387907313
ensembl	rs387907313
geneview	rs387907313
scholar	rs387907313
google	rs387907313
pharmgkb	rs387907313
gwascentral	rs387907313
openSNP	rs387907313
23andMe	rs387907313
SNPshot	rs387907313
SNPdbe	rs387907313
MSV3d	rs387907313
GWAS Ctlg	rs387907313

Max Magnitude

0

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,