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rs121434503

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121434503(C;T)
Make rs121434503(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position108753466
GeneRANBP2
is asnp
is mentioned by
dbSNPrs121434503
ebirs121434503
HLIrs121434503
Exacrs121434503
Varsomers121434503
Maprs121434503
PheGenIrs121434503
hapmaprs121434503
1000 genomesrs121434503
hgdprs121434503
ensemblrs121434503
gopubmedrs121434503
geneviewrs121434503
scholarrs121434503
googlers121434503
pharmgkbrs121434503
gwascentralrs121434503
openSNPrs121434503
23andMers121434503
23andMe allrs121434503
SNP Nexus

SNPshotrs121434503
SNPdbers121434503
MSV3drs121434503
GWAS Ctlgrs121434503
Max Magnitude0
OMIM601181
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434503(T;T)
Alt rs121434503(T;T)
Reference rs121434503(C;C)
Significance Other
Disease Encephalopathy
Variation info
Gene RANBP2
CLNDBN Encephalopathy, acute, infection-induced, 3, suceptibility to
Reversed 0
HGVS NC_000002.11:g.109369922C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008869.2,