rs10478694
From SNPedia
Merged into | rs1800997 |
Orientation | plus |
Stabilized | plus |
Make rs10478694(-;-) |
Make rs10478694(-;A) |
Make rs10478694(A;A) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 12290496 |
Gene | EDN1 |
is a | snp |
is | mentioned by |
dbSNP | rs10478694 |
dbSNP (classic) | rs10478694 |
ClinGen | rs10478694 |
ebi | rs10478694 |
HLI | rs10478694 |
Exac | rs10478694 |
Gnomad | rs10478694 |
Varsome | rs10478694 |
LitVar | rs10478694 |
Map | rs10478694 |
PheGenI | rs10478694 |
Biobank | rs10478694 |
1000 genomes | rs10478694 |
hgdp | rs10478694 |
ensembl | rs10478694 |
geneview | rs10478694 |
scholar | rs10478694 |
rs10478694 | |
pharmgkb | rs10478694 |
gwascentral | rs10478694 |
openSNP | rs10478694 |
23andMe | rs10478694 |
SNPshot | rs10478694 |
SNPdbe | rs10478694 |
MSV3d | rs10478694 |
GWAS Ctlg | rs10478694 |
Status | Merged into rs1800997 |
Max Magnitude | 0 |
[PMID 24747133] Association of Endothelin-1 Gene Polymorphisms with the Clinical Phenotype in Primary Nephrotic Syndrome of Children