rs147579680
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs147579680(C;T) |
Make rs147579680(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 63624124 |
Gene | DPY19L2 |
is a | snp |
is | mentioned by |
dbSNP | rs147579680 |
dbSNP (classic) | rs147579680 |
ClinGen | rs147579680 |
ebi | rs147579680 |
HLI | rs147579680 |
Exac | rs147579680 |
Gnomad | rs147579680 |
Varsome | rs147579680 |
LitVar | rs147579680 |
Map | rs147579680 |
PheGenI | rs147579680 |
Biobank | rs147579680 |
1000 genomes | rs147579680 |
hgdp | rs147579680 |
ensembl | rs147579680 |
geneview | rs147579680 |
scholar | rs147579680 |
rs147579680 | |
pharmgkb | rs147579680 |
gwascentral | rs147579680 |
openSNP | rs147579680 |
23andMe | rs147579680 |
SNPshot | rs147579680 |
SNPdbe | rs147579680 |
MSV3d | rs147579680 |
GWAS Ctlg | rs147579680 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147579680(T;T) |
Alt | rs147579680(T;T) |
Reference | Rs147579680(C;C) |
Significance | Pathogenic |
Disease | Spermatogenic failure 9 |
Variation | info |
Gene | DPY19L2 |
CLNDBN | Spermatogenic failure 9 |
Reversed | 0 |
HGVS | NC_000012.11:g.64017904C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000087741.4, |