rs786204637

Orientation

minus

Stabilized

minus

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

Make rs786204637(A;A)

Make rs786204637(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

119028193

Gene

SLC37A4

is a	snp
is	mentioned by
dbSNP	rs786204637
dbSNP (classic)	rs786204637
ClinGen	rs786204637
ebi	rs786204637
HLI	rs786204637
Exac	rs786204637
Gnomad	rs786204637
Varsome	rs786204637
LitVar	rs786204637
Map	rs786204637
PheGenI	rs786204637
Biobank	rs786204637
1000 genomes	rs786204637
hgdp	rs786204637
ensembl	rs786204637
geneview	rs786204637
scholar	rs786204637
google	rs786204637
pharmgkb	rs786204637
gwascentral	rs786204637
openSNP	rs786204637
23andMe	rs786204637
SNPshot	rs786204637
SNPdbe	rs786204637
MSV3d	rs786204637
GWAS Ctlg	rs786204637

Max Magnitude

0

ClinVar
Risk	rs786204637(A;A)
Alt	rs786204637(A;A)
Reference	Rs786204637(G;G)
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.118898903C>T
CLNSRC
CLNACC	RCV000169418.1,