rs111033666

Orientation

plus

Stabilized

plus

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

Make rs111033666(G;G)

Make rs111033666(G;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

34647504

Gene

GALT

is a	snp
is	mentioned by
dbSNP	rs111033666
dbSNP (classic)	rs111033666
ClinGen	rs111033666
ebi	rs111033666
HLI	rs111033666
Exac	rs111033666
Gnomad	rs111033666
Varsome	rs111033666
LitVar	rs111033666
Map	rs111033666
PheGenI	rs111033666
Biobank	rs111033666
1000 genomes	rs111033666
hgdp	rs111033666
ensembl	rs111033666
geneview	rs111033666
scholar	rs111033666
google	rs111033666
pharmgkb	rs111033666
gwascentral	rs111033666
openSNP	rs111033666
23andMe	rs111033666
SNPshot	rs111033666
SNPdbe	rs111033666
MSV3d	rs111033666
GWAS Ctlg	rs111033666

Max Magnitude

0

ClinVar
Risk	rs111033666(C;C) rs111033666(G;G)
Alt	rs111033666(C;C) rs111033666(G;G)
Reference	Rs111033666(T;T)
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.34647501T>C; NC_000009.11:g.34647501T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000022075.1, RCV000022074.1, RCV000482282.1,