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rs113994057

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994057(G;T)
Make rs113994057(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position184140120
GeneEIF2B5
is asnp
is mentioned by
dbSNPrs113994057
ebirs113994057
HLIrs113994057
Exacrs113994057
Varsomers113994057
Maprs113994057
PheGenIrs113994057
hapmaprs113994057
1000 genomesrs113994057
hgdprs113994057
ensemblrs113994057
gopubmedrs113994057
geneviewrs113994057
scholarrs113994057
googlers113994057
pharmgkbrs113994057
gwascentralrs113994057
openSNPrs113994057
23andMers113994057
23andMe allrs113994057
SNP Nexus

SNPshotrs113994057
SNPdbers113994057
MSV3drs113994057
GWAS Ctlgrs113994057
Max Magnitude0
ClinVar
Risk rs113994057(A,T;A,T)
Alt rs113994057(A,T;A,T)
Reference rs113994057(G;G)
Significance Untested
Disease
Variation info
Gene EIF2B5
CLNDBN
Reversed 0
HGVS NC_000003.11:g.183857908G>A; NC_000003.11:g.183857908G>T
CLNSRC
CLNACC


OMIM603896
Desc
Variant
Relatedalso