rs121908975

Orientation

minus

Stabilized

minus

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

Make rs121908975(G;T)

Make rs121908975(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

119025251

Gene

SLC37A4

is a	snp
is	mentioned by
dbSNP	rs121908975
dbSNP (classic)	rs121908975
ClinGen	rs121908975
ebi	rs121908975
HLI	rs121908975
Exac	rs121908975
Gnomad	rs121908975
Varsome	rs121908975
LitVar	rs121908975
Map	rs121908975
PheGenI	rs121908975
Biobank	rs121908975
1000 genomes	rs121908975
hgdp	rs121908975
ensembl	rs121908975
geneview	rs121908975
scholar	rs121908975
google	rs121908975
pharmgkb	rs121908975
gwascentral	rs121908975
openSNP	rs121908975
23andMe	rs121908975
SNPshot	rs121908975
SNPdbe	rs121908975
MSV3d	rs121908975
GWAS Ctlg	rs121908975

Max Magnitude

0

OMIM	602671
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908975(A;A) rs121908975(T;T)
Alt	rs121908975(A;A) rs121908975(T;T)
Reference	Rs121908975(G;G)
Significance	Pathogenic
Disease	Glucose-6-phosphate transport defect
Variation	info
Gene	SLC37A4
CLNDBN	Glucose-6-phosphate transport defect
Reversed	1
HGVS	NC_000011.9:g.118895961C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007331.3,