rs1057519828
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1057519828(A;A) |
Make rs1057519828(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 55143387 |
Gene | EGFR |
is a | snp |
is | mentioned by |
dbSNP | rs1057519828 |
dbSNP (classic) | rs1057519828 |
ClinGen | rs1057519828 |
ebi | rs1057519828 |
HLI | rs1057519828 |
Exac | rs1057519828 |
Gnomad | rs1057519828 |
Varsome | rs1057519828 |
LitVar | rs1057519828 |
Map | rs1057519828 |
PheGenI | rs1057519828 |
Biobank | rs1057519828 |
1000 genomes | rs1057519828 |
hgdp | rs1057519828 |
ensembl | rs1057519828 |
geneview | rs1057519828 |
scholar | rs1057519828 |
rs1057519828 | |
pharmgkb | rs1057519828 |
gwascentral | rs1057519828 |
openSNP | rs1057519828 |
23andMe | rs1057519828 |
SNPshot | rs1057519828 |
SNPdbe | rs1057519828 |
MSV3d | rs1057519828 |
GWAS Ctlg | rs1057519828 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057519828(A;A) |
Alt | rs1057519828(A;A) |
Reference | Rs1057519828(G;G) |
Significance | Probable-Pathogenic |
Disease | Neoplasm of brain |
Variation | info |
Gene | EGFR |
CLNDBN | Neoplasm of brain |
Reversed | 0 |
HGVS | NC_000007.13:g.55211080G>A |
CLNSRC | |
CLNACC | RCV000432019.1, |