rs121908979

Orientation

minus

Stabilized

minus

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

Make rs121908979(C;T)

Make rs121908979(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

119024957

Gene

SLC37A4

is a	snp
is	mentioned by
dbSNP	rs121908979
dbSNP (classic)	rs121908979
ClinGen	rs121908979
ebi	rs121908979
HLI	rs121908979
Exac	rs121908979
Gnomad	rs121908979
Varsome	rs121908979
LitVar	rs121908979
Map	rs121908979
PheGenI	rs121908979
Biobank	rs121908979
1000 genomes	rs121908979
hgdp	rs121908979
ensembl	rs121908979
geneview	rs121908979
scholar	rs121908979
google	rs121908979
pharmgkb	rs121908979
gwascentral	rs121908979
openSNP	rs121908979
23andMe	rs121908979
SNPshot	rs121908979
SNPdbe	rs121908979
MSV3d	rs121908979
GWAS Ctlg	rs121908979

Max Magnitude

0

OMIM	602671
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121908979(T;T)
Alt	rs121908979(T;T)
Reference	Rs121908979(C;C)
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.118895667G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007346.3,