rs414960
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs414960(A;A) |
Make rs414960(A;C) |
Make rs414960(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 53494586 |
is a | snp |
is | mentioned by |
dbSNP | rs414960 |
dbSNP (classic) | rs414960 |
ClinGen | rs414960 |
ebi | rs414960 |
HLI | rs414960 |
Exac | rs414960 |
Gnomad | rs414960 |
Varsome | rs414960 |
LitVar | rs414960 |
Map | rs414960 |
PheGenI | rs414960 |
Biobank | rs414960 |
1000 genomes | rs414960 |
hgdp | rs414960 |
ensembl | rs414960 |
geneview | rs414960 |
scholar | rs414960 |
rs414960 | |
pharmgkb | rs414960 |
gwascentral | rs414960 |
openSNP | rs414960 |
23andMe | rs414960 |
SNPshot | rs414960 |
SNPdbe | rs414960 |
MSV3d | rs414960 |
GWAS Ctlg | rs414960 |
GMAF | 0.3235 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 22177906] Development of multiplex assay with 16 SNPs on X chromosome for degraded samples