rs61865882
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs61865882(C;C) |
Make rs61865882(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 62812333 |
Gene | EGR2 |
is a | snp |
is | mentioned by |
dbSNP | rs61865882 |
dbSNP (classic) | rs61865882 |
ClinGen | rs61865882 |
ebi | rs61865882 |
HLI | rs61865882 |
Exac | rs61865882 |
Gnomad | rs61865882 |
Varsome | rs61865882 |
LitVar | rs61865882 |
Map | rs61865882 |
PheGenI | rs61865882 |
Biobank | rs61865882 |
1000 genomes | rs61865882 |
hgdp | rs61865882 |
ensembl | rs61865882 |
geneview | rs61865882 |
scholar | rs61865882 |
rs61865882 | |
pharmgkb | rs61865882 |
gwascentral | rs61865882 |
openSNP | rs61865882 |
23andMe | rs61865882 |
SNPshot | rs61865882 |
SNPdbe | rs61865882 |
MSV3d | rs61865882 |
GWAS Ctlg | rs61865882 |
GMAF | 0.07713 |
Max Magnitude | 0 |
[PMID 22089088] 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, |