rs508485
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs508485(C;C) |
Make rs508485(C;T) |
Make rs508485(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 94621313 |
Gene | LOC105369438, PIWIL4 |
is a | snp |
is | mentioned by |
dbSNP | rs508485 |
dbSNP (classic) | rs508485 |
ClinGen | rs508485 |
ebi | rs508485 |
HLI | rs508485 |
Exac | rs508485 |
Gnomad | rs508485 |
Varsome | rs508485 |
LitVar | rs508485 |
Map | rs508485 |
PheGenI | rs508485 |
Biobank | rs508485 |
1000 genomes | rs508485 |
hgdp | rs508485 |
ensembl | rs508485 |
geneview | rs508485 |
scholar | rs508485 |
rs508485 | |
pharmgkb | rs508485 |
gwascentral | rs508485 |
openSNP | rs508485 |
23andMe | rs508485 |
SNPshot | rs508485 |
SNPdbe | rs508485 |
MSV3d | rs508485 |
GWAS Ctlg | rs508485 |
GMAF | 0.4734 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20940137] Genetic variants in Piwi-interacting RNA pathway genes confer susceptibility to spermatogenic failure in a Chinese population