rs2237051
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs2237051(A;A) |
Make rs2237051(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 109980042 |
Gene | EGF |
is a | snp |
is | mentioned by |
dbSNP | rs2237051 |
dbSNP (classic) | rs2237051 |
ClinGen | rs2237051 |
ebi | rs2237051 |
HLI | rs2237051 |
Exac | rs2237051 |
Gnomad | rs2237051 |
Varsome | rs2237051 |
LitVar | rs2237051 |
Map | rs2237051 |
PheGenI | rs2237051 |
Biobank | rs2237051 |
1000 genomes | rs2237051 |
hgdp | rs2237051 |
ensembl | rs2237051 |
geneview | rs2237051 |
scholar | rs2237051 |
rs2237051 | |
pharmgkb | rs2237051 |
gwascentral | rs2237051 |
openSNP | rs2237051 |
23andMe | rs2237051 |
SNPshot | rs2237051 |
SNPdbe | rs2237051 |
MSV3d | rs2237051 |
GWAS Ctlg | rs2237051 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24754849] Polymorphism in the epidermal growth factor gene is associated with pre-eclampsia and low birthweight
[PMID 24945674] Genetic variants of EGF and VEGF predict prognosis of patients with advanced esophageal squamous cell carcinoma
ClinVar | |
---|---|
Risk | rs2237051(A;A) |
Alt | rs2237051(A;A) |
Reference | Rs2237051(G;G) |
Significance | Non-pathogenic |
Disease | Renal Hypomagnesemia |
Variation | info |
Gene | EGF |
CLNDBN | Renal Hypomagnesemia, Recessive |
Reversed | 0 |
HGVS | NC_000004.11:g.110901198G>A |
CLNSRC | |
CLNACC | RCV000261366.1, |
[PMID 31833563] A novel multi-locus genetic risk score identifies patients with higher risk of generalized aggressive periodontitis.
[PMID 31906817] Association between epidermal growth factor (EGF) and EGF receptor gene polymorphisms and end-stage renal disease and acute renal allograft rejection in a Korean population.