rs140880838
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs140880838(A;A) |
Make rs140880838(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 19 |
Position | 855988 |
Gene | ELANE |
is a | snp |
is | mentioned by |
dbSNP | rs140880838 |
dbSNP (classic) | rs140880838 |
ClinGen | rs140880838 |
ebi | rs140880838 |
HLI | rs140880838 |
Exac | rs140880838 |
Gnomad | rs140880838 |
Varsome | rs140880838 |
LitVar | rs140880838 |
Map | rs140880838 |
PheGenI | rs140880838 |
Biobank | rs140880838 |
1000 genomes | rs140880838 |
hgdp | rs140880838 |
ensembl | rs140880838 |
geneview | rs140880838 |
scholar | rs140880838 |
rs140880838 | |
pharmgkb | rs140880838 |
gwascentral | rs140880838 |
openSNP | rs140880838 |
23andMe | rs140880838 |
SNPshot | rs140880838 |
SNPdbe | rs140880838 |
MSV3d | rs140880838 |
GWAS Ctlg | rs140880838 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs140880838(A;A) |
Alt | rs140880838(A;A) |
Reference | Rs140880838(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ELANE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.855988G>A |
CLNSRC | |
CLNACC | RCV000255959.1, |