rs376518776
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs376518776(A;A) |
Make rs376518776(A;G) |
Make rs376518776(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 842051 |
Gene | DMRT1 |
is a | snp |
is | mentioned by |
dbSNP | rs376518776 |
dbSNP (classic) | rs376518776 |
ClinGen | rs376518776 |
ebi | rs376518776 |
HLI | rs376518776 |
Exac | rs376518776 |
Gnomad | rs376518776 |
Varsome | rs376518776 |
LitVar | rs376518776 |
Map | rs376518776 |
PheGenI | rs376518776 |
Biobank | rs376518776 |
1000 genomes | rs376518776 |
hgdp | rs376518776 |
ensembl | rs376518776 |
geneview | rs376518776 |
scholar | rs376518776 |
rs376518776 | |
pharmgkb | rs376518776 |
gwascentral | rs376518776 |
openSNP | rs376518776 |
23andMe | rs376518776 |
SNPshot | rs376518776 |
SNPdbe | rs376518776 |
MSV3d | rs376518776 |
GWAS Ctlg | rs376518776 |
Max Magnitude | 0 |
[PMID 26139570] Rare double sex and mab-3-related transcription factor 1 regulatory variants in severe spermatogenic failure