rs281865136

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs281865136(A;A)

Make rs281865136(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

62813562

Gene

EGR2

is a	snp
is	mentioned by
dbSNP	rs281865136
dbSNP (classic)	rs281865136
ClinGen	rs281865136
ebi	rs281865136
HLI	rs281865136
Exac	rs281865136
Gnomad	rs281865136
Varsome	rs281865136
LitVar	rs281865136
Map	rs281865136
PheGenI	rs281865136
Biobank	rs281865136
1000 genomes	rs281865136
hgdp	rs281865136
ensembl	rs281865136
geneview	rs281865136
scholar	rs281865136
google	rs281865136
pharmgkb	rs281865136
gwascentral	rs281865136
openSNP	rs281865136
23andMe	rs281865136
SNPshot	rs281865136
SNPdbe	rs281865136
MSV3d	rs281865136
GWAS Ctlg	rs281865136

Max Magnitude

0

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,