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rs121434504

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121434504(A;G)
Make rs121434504(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position108753474
GeneRANBP2
is asnp
is mentioned by
dbSNPrs121434504
ebirs121434504
HLIrs121434504
Exacrs121434504
Varsomers121434504
Maprs121434504
PheGenIrs121434504
hapmaprs121434504
1000 genomesrs121434504
hgdprs121434504
ensemblrs121434504
gopubmedrs121434504
geneviewrs121434504
scholarrs121434504
googlers121434504
pharmgkbrs121434504
gwascentralrs121434504
openSNPrs121434504
23andMers121434504
23andMe allrs121434504
SNP Nexus

SNPshotrs121434504
SNPdbers121434504
MSV3drs121434504
GWAS Ctlgrs121434504
Max Magnitude0
OMIM601181
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434504(G;G)
Alt rs121434504(G;G)
Reference rs121434504(A;A)
Significance Other
Disease Encephalopathy
Variation info
Gene RANBP2
CLNDBN Encephalopathy, acute, infection-induced, 3, suceptibility to
Reversed 0
HGVS NC_000002.11:g.109369930A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008870.2,