rs111033670

Orientation

plus

Stabilized

plus

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

Make rs111033670(A;A)

Make rs111033670(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

34647531

Gene

GALT

is a	snp
is	mentioned by
dbSNP	rs111033670
dbSNP (classic)	rs111033670
ClinGen	rs111033670
ebi	rs111033670
HLI	rs111033670
Exac	rs111033670
Gnomad	rs111033670
Varsome	rs111033670
LitVar	rs111033670
Map	rs111033670
PheGenI	rs111033670
Biobank	rs111033670
1000 genomes	rs111033670
hgdp	rs111033670
ensembl	rs111033670
geneview	rs111033670
scholar	rs111033670
google	rs111033670
pharmgkb	rs111033670
gwascentral	rs111033670
openSNP	rs111033670
23andMe	rs111033670
SNPshot	rs111033670
SNPdbe	rs111033670
MSV3d	rs111033670
GWAS Ctlg	rs111033670

Max Magnitude

0

ClinVar
Risk	rs111033670(A;A) rs111033670(C;C)
Alt	rs111033670(A;A) rs111033670(C;C)
Reference	Rs111033670(G;G)
Significance	Pathogenic
Disease	Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase not provided
Variation	info
Gene	GALT
CLNDBN	Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase not provided
Reversed	0
HGVS	NC_000009.11:g.34647528G>A; NC_000009.11:g.34647528G>C
CLNSRC	UniProtKB (protein) HGMD
CLNACC	RCV000022079.2, RCV000022080.2, RCV000078219.4,