rs1328641
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1328641(A;A) |
Make rs1328641(A;G) |
Make rs1328641(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 13 |
Position | 36170892 |
Gene | CCDC169-SOHLH2, SOHLH2 |
is a | snp |
is | mentioned by |
dbSNP | rs1328641 |
dbSNP (classic) | rs1328641 |
ClinGen | rs1328641 |
ebi | rs1328641 |
HLI | rs1328641 |
Exac | rs1328641 |
Gnomad | rs1328641 |
Varsome | rs1328641 |
LitVar | rs1328641 |
Map | rs1328641 |
PheGenI | rs1328641 |
Biobank | rs1328641 |
1000 genomes | rs1328641 |
hgdp | rs1328641 |
ensembl | rs1328641 |
geneview | rs1328641 |
scholar | rs1328641 |
rs1328641 | |
pharmgkb | rs1328641 |
gwascentral | rs1328641 |
openSNP | rs1328641 |
23andMe | rs1328641 |
SNPshot | rs1328641 |
SNPdbe | rs1328641 |
MSV3d | rs1328641 |
GWAS Ctlg | rs1328641 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25463635] Association of genetic variants in SOHLH1 and SOHLH2 with non-obstructive azoospermia risk in the Chinese population