rs7199196
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common genotype |
Make rs7199196(C;C) |
Make rs7199196(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 54315695 |
is a | snp |
is | mentioned by |
dbSNP | rs7199196 |
dbSNP (classic) | rs7199196 |
ClinGen | rs7199196 |
ebi | rs7199196 |
HLI | rs7199196 |
Exac | rs7199196 |
Gnomad | rs7199196 |
Varsome | rs7199196 |
LitVar | rs7199196 |
Map | rs7199196 |
PheGenI | rs7199196 |
Biobank | rs7199196 |
1000 genomes | rs7199196 |
hgdp | rs7199196 |
ensembl | rs7199196 |
geneview | rs7199196 |
scholar | rs7199196 |
rs7199196 | |
pharmgkb | rs7199196 |
gwascentral | rs7199196 |
openSNP | rs7199196 |
23andMe | rs7199196 |
SNPshot | rs7199196 |
SNPdbe | rs7199196 |
MSV3d | rs7199196 |
GWAS Ctlg | rs7199196 |
GMAF | 0.06933 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|