rs113994057
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs113994057(G;T) |
Make rs113994057(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 184140120 |
Gene | EIF2B5 |
is a | snp |
is | mentioned by |
dbSNP | rs113994057 |
dbSNP (classic) | rs113994057 |
ClinGen | rs113994057 |
ebi | rs113994057 |
HLI | rs113994057 |
Exac | rs113994057 |
Gnomad | rs113994057 |
Varsome | rs113994057 |
LitVar | rs113994057 |
Map | rs113994057 |
PheGenI | rs113994057 |
Biobank | rs113994057 |
1000 genomes | rs113994057 |
hgdp | rs113994057 |
ensembl | rs113994057 |
geneview | rs113994057 |
scholar | rs113994057 |
rs113994057 | |
pharmgkb | rs113994057 |
gwascentral | rs113994057 |
openSNP | rs113994057 |
23andMe | rs113994057 |
SNPshot | rs113994057 |
SNPdbe | rs113994057 |
MSV3d | rs113994057 |
GWAS Ctlg | rs113994057 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs113994057(A;A) rs113994057(T;T) |
Alt | rs113994057(A;A) rs113994057(T;T) |
Reference | Rs113994057(G;G) |
Significance | Untested |
Disease | |
Variation | info |
Gene | EIF2B5 |
CLNDBN | |
Reversed | 0 |
HGVS | NC_000003.11:g.183857908G>A; NC_000003.11:g.183857908G>T |
CLNSRC | |
CLNACC |