rs781784543

Orientation

plus

Stabilized

plus

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

Make rs781784543(A;A)

Make rs781784543(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

119026979

Gene

SLC37A4

is a	snp
is	mentioned by
dbSNP	rs781784543
dbSNP (classic)	rs781784543
ClinGen	rs781784543
ebi	rs781784543
HLI	rs781784543
Exac	rs781784543
Gnomad	rs781784543
Varsome	rs781784543
LitVar	rs781784543
Map	rs781784543
PheGenI	rs781784543
Biobank	rs781784543
1000 genomes	rs781784543
hgdp	rs781784543
ensembl	rs781784543
geneview	rs781784543
scholar	rs781784543
google	rs781784543
pharmgkb	rs781784543
gwascentral	rs781784543
openSNP	rs781784543
23andMe	rs781784543
SNPshot	rs781784543
SNPdbe	rs781784543
MSV3d	rs781784543
GWAS Ctlg	rs781784543

Max Magnitude

0

ClinVar
Risk	rs781784543(A;A)
Alt	rs781784543(A;A)
Reference	Rs781784543(G;G)
Significance	Pathogenic
Disease	Glucose-6-phosphate transport defect not provided
Variation	info
Gene	SLC37A4
CLNDBN	Glucose-6-phosphate transport defect not provided
Reversed	0
HGVS	NC_000011.9:g.118897689G>A
CLNSRC
CLNACC	RCV000169082.1, RCV000300702.1,