rs111033765

Orientation

plus

Stabilized

plus

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

Make rs111033765(A;G)

Make rs111033765(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

34648886

Gene

GALT

is a	snp
is	mentioned by
dbSNP	rs111033765
dbSNP (classic)	rs111033765
ClinGen	rs111033765
ebi	rs111033765
HLI	rs111033765
Exac	rs111033765
Gnomad	rs111033765
Varsome	rs111033765
LitVar	rs111033765
Map	rs111033765
PheGenI	rs111033765
Biobank	rs111033765
1000 genomes	rs111033765
hgdp	rs111033765
ensembl	rs111033765
geneview	rs111033765
scholar	rs111033765
google	rs111033765
pharmgkb	rs111033765
gwascentral	rs111033765
openSNP	rs111033765
23andMe	rs111033765
SNPshot	rs111033765
SNPdbe	rs111033765
MSV3d	rs111033765
GWAS Ctlg	rs111033765

Max Magnitude

0

ClinVar
Risk	rs111033765(G;G)
Alt	rs111033765(G;G)
Reference	Rs111033765(A;A)
Significance	Pathogenic
Disease	Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase not specified
Variation	info
Gene	GALT
CLNDBN	Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase not specified
Reversed	0
HGVS	NC_000009.11:g.34648883A>G
CLNSRC	ARUP GALT
CLNACC	RCV000022208.1, RCV000180101.2,