rs745455816
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs745455816(A;A) |
Make rs745455816(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 853345 |
Gene | ELANE |
is a | snp |
is | mentioned by |
dbSNP | rs745455816 |
dbSNP (classic) | rs745455816 |
ClinGen | rs745455816 |
ebi | rs745455816 |
HLI | rs745455816 |
Exac | rs745455816 |
Gnomad | rs745455816 |
Varsome | rs745455816 |
LitVar | rs745455816 |
Map | rs745455816 |
PheGenI | rs745455816 |
Biobank | rs745455816 |
1000 genomes | rs745455816 |
hgdp | rs745455816 |
ensembl | rs745455816 |
geneview | rs745455816 |
scholar | rs745455816 |
rs745455816 | |
pharmgkb | rs745455816 |
gwascentral | rs745455816 |
openSNP | rs745455816 |
23andMe | rs745455816 |
SNPshot | rs745455816 |
SNPdbe | rs745455816 |
MSV3d | rs745455816 |
GWAS Ctlg | rs745455816 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745455816(A;A) rs745455816(T;T) |
Alt | rs745455816(A;A) rs745455816(T;T) |
Reference | Rs745455816(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ELANE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.853345G>T |
CLNSRC | |
CLNACC | RCV000478914.1, |