rs111033825

Orientation

plus

Stabilized

plus

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

Make rs111033825(-;G)

Make rs111033825(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

34648427

Gene

GALT

is a	snp
is	mentioned by
dbSNP	rs111033825
dbSNP (classic)	rs111033825
ClinGen	rs111033825
ebi	rs111033825
HLI	rs111033825
Exac	rs111033825
Gnomad	rs111033825
Varsome	rs111033825
LitVar	rs111033825
Map	rs111033825
PheGenI	rs111033825
Biobank	rs111033825
1000 genomes	rs111033825
hgdp	rs111033825
ensembl	rs111033825
geneview	rs111033825
scholar	rs111033825
google	rs111033825
pharmgkb	rs111033825
gwascentral	rs111033825
openSNP	rs111033825
23andMe	rs111033825
SNPshot	rs111033825
SNPdbe	rs111033825
MSV3d	rs111033825
GWAS Ctlg	rs111033825

Max Magnitude

0

ClinVar
Risk	rs111033825(G;G)
Alt	rs111033825(G;G)
Reference	Rs111033825(-;-)
Significance	Pathogenic
Disease	Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Variation	info
Gene	GALT
CLNDBN	Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase
Reversed	0
HGVS	NC_000009.11:g.34648424dupG
CLNSRC	ClinVar
CLNACC	RCV000022177.1,