rs786204740

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs786204740(A;G)

Make rs786204740(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

119029369

Gene

SLC37A4

is a	snp
is	mentioned by
dbSNP	rs786204740
dbSNP (classic)	rs786204740
ClinGen	rs786204740
ebi	rs786204740
HLI	rs786204740
Exac	rs786204740
Gnomad	rs786204740
Varsome	rs786204740
LitVar	rs786204740
Map	rs786204740
PheGenI	rs786204740
Biobank	rs786204740
1000 genomes	rs786204740
hgdp	rs786204740
ensembl	rs786204740
geneview	rs786204740
scholar	rs786204740
google	rs786204740
pharmgkb	rs786204740
gwascentral	rs786204740
openSNP	rs786204740
23andMe	rs786204740
SNPshot	rs786204740
SNPdbe	rs786204740
MSV3d	rs786204740
GWAS Ctlg	rs786204740

Max Magnitude

0

ClinVar
Risk	rs786204740(G;G)
Alt	rs786204740(G;G)
Reference	Rs786204740(A;A)
Significance	Probable-Pathogenic
Disease	Glucose-6-phosphate transport defect
Variation	info
Gene	SLC37A4
CLNDBN	Glucose-6-phosphate transport defect
Reversed	1
HGVS	NC_000011.9:g.118900079T>C
CLNSRC
CLNACC	RCV000169589.1,