rs5990560
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5990560(A;A) |
Make rs5990560(A;T) |
Make rs5990560(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 96406563 |
is a | snp |
is | mentioned by |
dbSNP | rs5990560 |
dbSNP (classic) | rs5990560 |
ClinGen | rs5990560 |
ebi | rs5990560 |
HLI | rs5990560 |
Exac | rs5990560 |
Gnomad | rs5990560 |
Varsome | rs5990560 |
LitVar | rs5990560 |
Map | rs5990560 |
PheGenI | rs5990560 |
Biobank | rs5990560 |
1000 genomes | rs5990560 |
hgdp | rs5990560 |
ensembl | rs5990560 |
geneview | rs5990560 |
scholar | rs5990560 |
rs5990560 | |
pharmgkb | rs5990560 |
gwascentral | rs5990560 |
openSNP | rs5990560 |
23andMe | rs5990560 |
SNPshot | rs5990560 |
SNPdbe | rs5990560 |
MSV3d | rs5990560 |
GWAS Ctlg | rs5990560 |
GMAF | 0.3567 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 22177906] Development of multiplex assay with 16 SNPs on X chromosome for degraded samples