rs144424711
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs144424711(C;C) |
Make rs144424711(C;T) |
Make rs144424711(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 16 |
Position | 85918417 |
Gene | IRF8, MIR6774 |
is a | snp |
is | mentioned by |
dbSNP | rs144424711 |
dbSNP (classic) | rs144424711 |
ClinGen | rs144424711 |
ebi | rs144424711 |
HLI | rs144424711 |
Exac | rs144424711 |
Gnomad | rs144424711 |
Varsome | rs144424711 |
LitVar | rs144424711 |
Map | rs144424711 |
PheGenI | rs144424711 |
Biobank | rs144424711 |
1000 genomes | rs144424711 |
hgdp | rs144424711 |
ensembl | rs144424711 |
geneview | rs144424711 |
scholar | rs144424711 |
rs144424711 | |
pharmgkb | rs144424711 |
gwascentral | rs144424711 |
openSNP | rs144424711 |
23andMe | rs144424711 |
SNPshot | rs144424711 |
SNPdbe | rs144424711 |
MSV3d | rs144424711 |
GWAS Ctlg | rs144424711 |
Max Magnitude | 0 |
OMIM pathogenic variant