rs5959408
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5959408(A;A) |
Make rs5959408(A;G) |
Make rs5959408(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 79658774 |
is a | snp |
is | mentioned by |
dbSNP | rs5959408 |
dbSNP (classic) | rs5959408 |
ClinGen | rs5959408 |
ebi | rs5959408 |
HLI | rs5959408 |
Exac | rs5959408 |
Gnomad | rs5959408 |
Varsome | rs5959408 |
LitVar | rs5959408 |
Map | rs5959408 |
PheGenI | rs5959408 |
Biobank | rs5959408 |
1000 genomes | rs5959408 |
hgdp | rs5959408 |
ensembl | rs5959408 |
geneview | rs5959408 |
scholar | rs5959408 |
rs5959408 | |
pharmgkb | rs5959408 |
gwascentral | rs5959408 |
openSNP | rs5959408 |
23andMe | rs5959408 |
SNPshot | rs5959408 |
SNPdbe | rs5959408 |
MSV3d | rs5959408 |
GWAS Ctlg | rs5959408 |
GMAF | 0.3984 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22177906] Development of multiplex assay with 16 SNPs on X chromosome for degraded samples