rs3826784

Orientation

plus

Stabilized

plus

Make rs3826784(A;A)

Make rs3826784(A;G)

Make rs3826784(G;G)

Reference

GRCh38 38.1/142

Chromosome

19

Position

10116334

Gene

EIF3G

is a	snp
is	mentioned by
dbSNP	rs3826784
dbSNP (classic)	rs3826784
ClinGen	rs3826784
ebi	rs3826784
HLI	rs3826784
Exac	rs3826784
Gnomad	rs3826784
Varsome	rs3826784
LitVar	rs3826784
Map	rs3826784
PheGenI	rs3826784
Biobank	rs3826784
1000 genomes	rs3826784
hgdp	rs3826784
ensembl	rs3826784
geneview	rs3826784
scholar	rs3826784
google	rs3826784
pharmgkb	rs3826784
gwascentral	rs3826784
openSNP	rs3826784
23andMe	rs3826784
SNPshot	rs3826784
SNPdbe	rs3826784
MSV3d	rs3826784
GWAS Ctlg	rs3826784

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 25669430] EIF3G is associated with narcolepsy across ethnicities

ClinVar
Risk	rs3826784(G;G)
Alt	rs3826784(G;G)
Reference	rs3826784(A;A)
Significance	Other
Disease	Cataplexy and narcolepsy
Variation	info
Gene	EIF3G
CLNDBN	Cataplexy and narcolepsy
Reversed	0
HGVS	NC_000019.9:g.10227010A>G
CLNSRC
CLNACC	RCV000161133.1,