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rs140280672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140280672(C;T)
Make rs140280672(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position108768038
GeneRANBP2
is asnp
is mentioned by
dbSNPrs140280672
dbSNP (old)rs140280672
ClinGenrs140280672
ebirs140280672
HLIrs140280672
Exacrs140280672
Gnomadrs140280672
Varsomers140280672
LitVarrs140280672
Maprs140280672
PheGenIrs140280672
Biobankrs140280672
1000 genomesrs140280672
hgdprs140280672
ensemblrs140280672
gopubmedrs140280672
geneviewrs140280672
scholarrs140280672
googlers140280672
pharmgkbrs140280672
gwascentralrs140280672
openSNPrs140280672
23andMers140280672
23andMe allrs140280672
SNPshotrs140280672
SNPdbers140280672
MSV3drs140280672
GWAS Ctlgrs140280672
Max Magnitude0
ClinVar
Risk rs140280672(T;T)
Alt rs140280672(T;T)
Reference Rs140280672(C;C)
Significance Probable-Pathogenic
Disease not specified Encephalopathy
Variation info
Gene RANBP2
CLNDBN not specified Encephalopathy, acute, infection-induced, 3, suceptibility to
Reversed 0
HGVS NC_000002.11:g.109384494C>T
CLNSRC
CLNACC RCV000419020.1, RCV000445589.1,