rs184770596

Orientation

plus

Stabilized

plus

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

Make rs184770596(C;G)

Make rs184770596(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

73938978

Gene

DGUOK

is a	snp
is	mentioned by
dbSNP	rs184770596
dbSNP (classic)	rs184770596
ClinGen	rs184770596
ebi	rs184770596
HLI	rs184770596
Exac	rs184770596
Gnomad	rs184770596
Varsome	rs184770596
LitVar	rs184770596
Map	rs184770596
PheGenI	rs184770596
Biobank	rs184770596
1000 genomes	rs184770596
hgdp	rs184770596
ensembl	rs184770596
geneview	rs184770596
scholar	rs184770596
google	rs184770596
pharmgkb	rs184770596
gwascentral	rs184770596
openSNP	rs184770596
23andMe	rs184770596
SNPshot	rs184770596
SNPdbe	rs184770596
MSV3d	rs184770596
GWAS Ctlg	rs184770596

Max Magnitude

0

ClinVar
Risk	rs184770596(G;G)
Alt	rs184770596(G;G)
Reference	Rs184770596(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases not specified
Variation	info
Gene	DGUOK
CLNDBN	Inborn genetic diseases not specified
Reversed	0
HGVS	NC_000002.11:g.74166105C>G
CLNSRC
CLNACC	RCV000190772.1, RCV000482950.1,