rs1057520674
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1057520674(G;T) |
Make rs1057520674(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 44894419 |
Gene | EFTUD2 |
is a | snp |
is | mentioned by |
dbSNP | rs1057520674 |
dbSNP (classic) | rs1057520674 |
ClinGen | rs1057520674 |
ebi | rs1057520674 |
HLI | rs1057520674 |
Exac | rs1057520674 |
Gnomad | rs1057520674 |
Varsome | rs1057520674 |
LitVar | rs1057520674 |
Map | rs1057520674 |
PheGenI | rs1057520674 |
Biobank | rs1057520674 |
1000 genomes | rs1057520674 |
hgdp | rs1057520674 |
ensembl | rs1057520674 |
geneview | rs1057520674 |
scholar | rs1057520674 |
rs1057520674 | |
pharmgkb | rs1057520674 |
gwascentral | rs1057520674 |
openSNP | rs1057520674 |
23andMe | rs1057520674 |
SNPshot | rs1057520674 |
SNPdbe | rs1057520674 |
MSV3d | rs1057520674 |
GWAS Ctlg | rs1057520674 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057520674(T;T) |
Alt | rs1057520674(T;T) |
Reference | Rs1057520674(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | EFTUD2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.42971787C>A |
CLNSRC | |
CLNACC | RCV000427380.1, |