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rs113994069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994069(C;C)
Make rs113994069(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position184140590
GeneEIF2B5
is asnp
is mentioned by
dbSNPrs113994069
ebirs113994069
HLIrs113994069
Exacrs113994069
Varsomers113994069
Maprs113994069
PheGenIrs113994069
hapmaprs113994069
1000 genomesrs113994069
hgdprs113994069
ensemblrs113994069
gopubmedrs113994069
geneviewrs113994069
scholarrs113994069
googlers113994069
pharmgkbrs113994069
gwascentralrs113994069
openSNPrs113994069
23andMers113994069
23andMe allrs113994069
SNP Nexus

SNPshotrs113994069
SNPdbers113994069
MSV3drs113994069
GWAS Ctlgrs113994069
Max Magnitude0
ClinVar
Risk rs113994069(A,C,T;A,C,T)
Alt rs113994069(A,C,T;A,C,T)
Reference rs113994069(G;G)
Significance Untested
Disease
Variation info
Gene EIF2B5
CLNDBN
Reversed 0
HGVS NC_000003.11:g.183858378G>A; NC_000003.11:g.183858378G>C; NC_000003.11:g.183858378G>T
CLNSRC
CLNACC


OMIM603896
Desc
Variant
Relatedalso