rs879255272
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TAAACTTGCTCAACGACATCGTGA;TAAACTTGCTCAACGACATCGTGA) | 0 | common in clinvar |
Make rs879255272(-;-) |
Make rs879255272(-;AAACTTGCTCAACGACATCGTGAT) |
Make rs879255272(AAACTTGCTCAACGACATCGTGAT;AAACTTGCTCAACGACATCGTGAT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 853373 |
Gene | ELANE |
is a | snp |
is | mentioned by |
dbSNP | rs879255272 |
dbSNP (classic) | rs879255272 |
ClinGen | rs879255272 |
ebi | rs879255272 |
HLI | rs879255272 |
Exac | rs879255272 |
Gnomad | rs879255272 |
Varsome | rs879255272 |
LitVar | rs879255272 |
Map | rs879255272 |
PheGenI | rs879255272 |
Biobank | rs879255272 |
1000 genomes | rs879255272 |
hgdp | rs879255272 |
ensembl | rs879255272 |
geneview | rs879255272 |
scholar | rs879255272 |
rs879255272 | |
pharmgkb | rs879255272 |
gwascentral | rs879255272 |
openSNP | rs879255272 |
23andMe | rs879255272 |
SNPshot | rs879255272 |
SNPdbe | rs879255272 |
MSV3d | rs879255272 |
GWAS Ctlg | rs879255272 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255272(-;-) |
Alt | rs879255272(-;-) |
Reference | Rs879255272(TAAACTTGCTCAACGACATCGTGA;TAAACTTGCTCAACGACATCGTGA) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ELANE |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.853373_853396del24 |
CLNSRC | |
CLNACC | RCV000234597.1, |