rs199659114
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs199659114(A;A) |
Make rs199659114(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 855775 |
Gene | ELANE |
is a | snp |
is | mentioned by |
dbSNP | rs199659114 |
dbSNP (classic) | rs199659114 |
ClinGen | rs199659114 |
ebi | rs199659114 |
HLI | rs199659114 |
Exac | rs199659114 |
Gnomad | rs199659114 |
Varsome | rs199659114 |
LitVar | rs199659114 |
Map | rs199659114 |
PheGenI | rs199659114 |
Biobank | rs199659114 |
1000 genomes | rs199659114 |
hgdp | rs199659114 |
ensembl | rs199659114 |
geneview | rs199659114 |
scholar | rs199659114 |
rs199659114 | |
pharmgkb | rs199659114 |
gwascentral | rs199659114 |
openSNP | rs199659114 |
23andMe | rs199659114 |
SNPshot | rs199659114 |
SNPdbe | rs199659114 |
MSV3d | rs199659114 |
GWAS Ctlg | rs199659114 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199659114(A;A) |
Alt | rs199659114(A;A) |
Reference | Rs199659114(G;G) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | ELANE |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000019.9:g.855775G>A |
CLNSRC | |
CLNACC | RCV000227502.2, |