rs16889859
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs16889859(A;G) |
Make rs16889859(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 78316148 |
Gene | LOC105377865 |
is a | snp |
is | mentioned by |
dbSNP | rs16889859 |
dbSNP (classic) | rs16889859 |
ClinGen | rs16889859 |
ebi | rs16889859 |
HLI | rs16889859 |
Exac | rs16889859 |
Gnomad | rs16889859 |
Varsome | rs16889859 |
LitVar | rs16889859 |
Map | rs16889859 |
PheGenI | rs16889859 |
Biobank | rs16889859 |
1000 genomes | rs16889859 |
hgdp | rs16889859 |
ensembl | rs16889859 |
geneview | rs16889859 |
scholar | rs16889859 |
rs16889859 | |
pharmgkb | rs16889859 |
gwascentral | rs16889859 |
openSNP | rs16889859 |
23andMe | rs16889859 |
SNPshot | rs16889859 |
SNPdbe | rs16889859 |
MSV3d | rs16889859 |
GWAS Ctlg | rs16889859 |
GMAF | 0.0955 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Here to enable genosets gs217 and gs218 which look for a CNV