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rs3826784

From SNPedia

Orientationplus
Stabilizedplus
Make rs3826784(A;A)
Make rs3826784(A;G)
Make rs3826784(G;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position10116334
GeneEIF3G
is asnp
is mentioned by
dbSNPrs3826784
ebirs3826784
HLIrs3826784
Exacrs3826784
Varsomers3826784
Maprs3826784
PheGenIrs3826784
hapmaprs3826784
1000 genomesrs3826784
hgdprs3826784
ensemblrs3826784
gopubmedrs3826784
geneviewrs3826784
scholarrs3826784
googlers3826784
pharmgkbrs3826784
gwascentralrs3826784
openSNPrs3826784
23andMers3826784
23andMe allrs3826784
SNP Nexus

SNPshotrs3826784
SNPdbers3826784
MSV3drs3826784
GWAS Ctlgrs3826784
Max Magnitude
? (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,