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rs281865136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865136(A;A)
Make rs281865136(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position62813562
GeneEGR2
is asnp
is mentioned by
dbSNPrs281865136
ebirs281865136
HLIrs281865136
Exacrs281865136
Varsomers281865136
Maprs281865136
PheGenIrs281865136
hapmaprs281865136
1000 genomesrs281865136
hgdprs281865136
ensemblrs281865136
gopubmedrs281865136
geneviewrs281865136
scholarrs281865136
googlers281865136
pharmgkbrs281865136
gwascentralrs281865136
openSNPrs281865136
23andMers281865136
23andMe allrs281865136
SNP Nexus

SNPshotrs281865136
SNPdbers281865136
MSV3drs281865136
GWAS Ctlgrs281865136
Max Magnitude0
ClinVar
Risk rs281865136(A;A)
Alt rs281865136(A;A)
Reference rs281865136(G;G)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene EGR2
CLNDBN Charcot-Marie-Tooth disease, demyelinating, type 1d
Reversed 1
HGVS NC_000010.10:g.64573322C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000033900.2,