rs6630351
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6630351(A;A) |
Make rs6630351(A;G) |
Make rs6630351(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 27086968 |
is a | snp |
is | mentioned by |
dbSNP | rs6630351 |
dbSNP (classic) | rs6630351 |
ClinGen | rs6630351 |
ebi | rs6630351 |
HLI | rs6630351 |
Exac | rs6630351 |
Gnomad | rs6630351 |
Varsome | rs6630351 |
LitVar | rs6630351 |
Map | rs6630351 |
PheGenI | rs6630351 |
Biobank | rs6630351 |
1000 genomes | rs6630351 |
hgdp | rs6630351 |
ensembl | rs6630351 |
geneview | rs6630351 |
scholar | rs6630351 |
rs6630351 | |
pharmgkb | rs6630351 |
gwascentral | rs6630351 |
openSNP | rs6630351 |
23andMe | rs6630351 |
SNPshot | rs6630351 |
SNPdbe | rs6630351 |
MSV3d | rs6630351 |
GWAS Ctlg | rs6630351 |
GMAF | 0.367 |
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