rs757556226
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs757556226(A;A) |
Make rs757556226(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 63488308 |
Gene | EEF1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs757556226 |
dbSNP (classic) | rs757556226 |
ClinGen | rs757556226 |
ebi | rs757556226 |
HLI | rs757556226 |
Exac | rs757556226 |
Gnomad | rs757556226 |
Varsome | rs757556226 |
LitVar | rs757556226 |
Map | rs757556226 |
PheGenI | rs757556226 |
Biobank | rs757556226 |
1000 genomes | rs757556226 |
hgdp | rs757556226 |
ensembl | rs757556226 |
geneview | rs757556226 |
scholar | rs757556226 |
rs757556226 | |
pharmgkb | rs757556226 |
gwascentral | rs757556226 |
openSNP | rs757556226 |
23andMe | rs757556226 |
SNPshot | rs757556226 |
SNPdbe | rs757556226 |
MSV3d | rs757556226 |
GWAS Ctlg | rs757556226 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs757556226(A;A) |
Alt | rs757556226(A;A) |
Reference | Rs757556226(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | EEF1A2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.62119661G>A |
CLNSRC | |
CLNACC | RCV000427894.1, |