Have questions? Visit https://www.reddit.com/r/SNPedia

rs113994063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113994063(C;G)
Make rs113994063(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position184140517
GeneEIF2B5
is asnp
is mentioned by
dbSNPrs113994063
ebirs113994063
HLIrs113994063
Exacrs113994063
Varsomers113994063
Maprs113994063
PheGenIrs113994063
hapmaprs113994063
1000 genomesrs113994063
hgdprs113994063
ensemblrs113994063
gopubmedrs113994063
geneviewrs113994063
scholarrs113994063
googlers113994063
pharmgkbrs113994063
gwascentralrs113994063
openSNPrs113994063
23andMers113994063
23andMe allrs113994063
SNP Nexus

SNPshotrs113994063
SNPdbers113994063
MSV3drs113994063
GWAS Ctlgrs113994063
Max Magnitude0
ClinVar
Risk rs113994063(G,T;G,T)
Alt rs113994063(G,T;G,T)
Reference rs113994063(C;C)
Significance Untested
Disease
Variation info
Gene EIF2B5
CLNDBN
Reversed 0
HGVS NC_000003.11:g.183858305C>G; NC_000003.11:g.183858305C>T
CLNSRC
CLNACC


OMIM603896
Desc
Variant
Relatedalso