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rs121434502

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121434502(C;T)
Make rs121434502(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position108751993
GeneRANBP2
is asnp
is mentioned by
dbSNPrs121434502
ebirs121434502
HLIrs121434502
Exacrs121434502
Varsomers121434502
Maprs121434502
PheGenIrs121434502
hapmaprs121434502
1000 genomesrs121434502
hgdprs121434502
ensemblrs121434502
gopubmedrs121434502
geneviewrs121434502
scholarrs121434502
googlers121434502
pharmgkbrs121434502
gwascentralrs121434502
openSNPrs121434502
23andMers121434502
23andMe allrs121434502
SNP Nexus

SNPshotrs121434502
SNPdbers121434502
MSV3drs121434502
GWAS Ctlgrs121434502
Max Magnitude0
OMIM601181
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434502(T;T)
Alt rs121434502(T;T)
Reference rs121434502(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.109368449C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008868.2,