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rs61865882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs61865882(C;C)
Make rs61865882(C;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position62812333
GeneEGR2
is asnp
is mentioned by
dbSNPrs61865882
dbSNP (classic)rs61865882
ClinGenrs61865882
ebirs61865882
HLIrs61865882
Exacrs61865882
Gnomadrs61865882
Varsomers61865882
LitVarrs61865882
Maprs61865882
PheGenIrs61865882
Biobankrs61865882
1000 genomesrs61865882
hgdprs61865882
ensemblrs61865882
geneviewrs61865882
scholarrs61865882
googlers61865882
pharmgkbrs61865882
gwascentralrs61865882
openSNPrs61865882
23andMers61865882
SNPshotrs61865882
SNPdbers61865882
MSV3drs61865882
GWAS Ctlgrs61865882
GMAF0.07713
Max Magnitude0

[PMID 22089088OA-icon.png] Genetic association of the EGR2 gene with bipolar disorder in Korea

ClinVar
Risk rs61865882(C;C)
Alt rs61865882(C;C)
Reference Rs61865882(T;T)
Significance Probable-non-pathogenic
Disease Charcot-Marie-Tooth
Variation info
Gene EGR2
CLNDBN Charcot-Marie-Tooth, Type 1
Reversed 0
HGVS NC_000010.10:g.64572093T>C
CLNSRC
CLNACC RCV000382555.1,