rs111033661

Orientation

plus

Stabilized

plus

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

Make rs111033661(A;G)

Make rs111033661(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

34647490

Gene

GALT

is a	snp
is	mentioned by
dbSNP	rs111033661
dbSNP (classic)	rs111033661
ClinGen	rs111033661
ebi	rs111033661
HLI	rs111033661
Exac	rs111033661
Gnomad	rs111033661
Varsome	rs111033661
LitVar	rs111033661
Map	rs111033661
PheGenI	rs111033661
Biobank	rs111033661
1000 genomes	rs111033661
hgdp	rs111033661
ensembl	rs111033661
geneview	rs111033661
scholar	rs111033661
google	rs111033661
pharmgkb	rs111033661
gwascentral	rs111033661
openSNP	rs111033661
23andMe	rs111033661
SNPshot	rs111033661
SNPdbe	rs111033661
MSV3d	rs111033661
GWAS Ctlg	rs111033661

Max Magnitude

0

ClinVar
Risk	rs111033661(G;G)
Alt	rs111033661(G;G)
Reference	Rs111033661(A;A)
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.34647487A>G
CLNSRC	ARUP GALT
CLNACC	RCV000022073.5, RCV000185912.2,