rs10494778
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs10494778(A;G) |
Make rs10494778(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 198558976 |
is a | snp |
is | mentioned by |
dbSNP | rs10494778 |
dbSNP (classic) | rs10494778 |
ClinGen | rs10494778 |
ebi | rs10494778 |
HLI | rs10494778 |
Exac | rs10494778 |
Gnomad | rs10494778 |
Varsome | rs10494778 |
LitVar | rs10494778 |
Map | rs10494778 |
PheGenI | rs10494778 |
Biobank | rs10494778 |
1000 genomes | rs10494778 |
hgdp | rs10494778 |
ensembl | rs10494778 |
geneview | rs10494778 |
scholar | rs10494778 |
rs10494778 | |
pharmgkb | rs10494778 |
gwascentral | rs10494778 |
openSNP | rs10494778 |
23andMe | rs10494778 |
SNPshot | rs10494778 |
SNPdbe | rs10494778 |
MSV3d | rs10494778 |
GWAS Ctlg | rs10494778 |
GMAF | 0.0955 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|