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rs113994028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994028(A;A)
Make rs113994028(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position27368104
GeneEIF2B4
is asnp
is mentioned by
dbSNPrs113994028
ebirs113994028
HLIrs113994028
Exacrs113994028
Varsomers113994028
Maprs113994028
PheGenIrs113994028
hapmaprs113994028
1000 genomesrs113994028
hgdprs113994028
ensemblrs113994028
gopubmedrs113994028
geneviewrs113994028
scholarrs113994028
googlers113994028
pharmgkbrs113994028
gwascentralrs113994028
openSNPrs113994028
23andMers113994028
23andMe allrs113994028
SNP Nexus

SNPshotrs113994028
SNPdbers113994028
MSV3drs113994028
GWAS Ctlgrs113994028
Max Magnitude0
ClinVar
Risk rs113994028(A;A)
Alt rs113994028(A;A)
Reference rs113994028(G;G)
Significance Pathogenic
Disease Leukoencephalopathy with vanishing white matter
Variation info
Gene EIF2B4
CLNDBN Leukoencephalopathy with vanishing white matter
Reversed 1
HGVS NC_000002.11:g.27590971C>T
CLNSRC
CLNACC


OMIM603896
Desc
Variant
Relatedalso