rs4132871
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4132871(C;C) |
Make rs4132871(C;T) |
Make rs4132871(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 135468448 |
is a | snp |
is | mentioned by |
dbSNP | rs4132871 |
dbSNP (classic) | rs4132871 |
ClinGen | rs4132871 |
ebi | rs4132871 |
HLI | rs4132871 |
Exac | rs4132871 |
Gnomad | rs4132871 |
Varsome | rs4132871 |
LitVar | rs4132871 |
Map | rs4132871 |
PheGenI | rs4132871 |
Biobank | rs4132871 |
1000 genomes | rs4132871 |
hgdp | rs4132871 |
ensembl | rs4132871 |
geneview | rs4132871 |
scholar | rs4132871 |
rs4132871 | |
pharmgkb | rs4132871 |
gwascentral | rs4132871 |
openSNP | rs4132871 |
23andMe | rs4132871 |
SNPshot | rs4132871 |
SNPdbe | rs4132871 |
MSV3d | rs4132871 |
GWAS Ctlg | rs4132871 |
GMAF | 0.4135 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22177906] Development of multiplex assay with 16 SNPs on X chromosome for degraded samples