rs587777206
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(G;G) | 0 | common in clinvar |
Make rs587777206(A;A) |
Make rs587777206(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 12 |
Position | 63624101 |
Gene | DPY19L2 |
is a | snp |
is | mentioned by |
dbSNP | rs587777206 |
dbSNP (classic) | rs587777206 |
ClinGen | rs587777206 |
ebi | rs587777206 |
HLI | rs587777206 |
Exac | rs587777206 |
Gnomad | rs587777206 |
Varsome | rs587777206 |
LitVar | rs587777206 |
Map | rs587777206 |
PheGenI | rs587777206 |
Biobank | rs587777206 |
1000 genomes | rs587777206 |
hgdp | rs587777206 |
ensembl | rs587777206 |
geneview | rs587777206 |
scholar | rs587777206 |
rs587777206 | |
pharmgkb | rs587777206 |
gwascentral | rs587777206 |
openSNP | rs587777206 |
23andMe | rs587777206 |
SNPshot | rs587777206 |
SNPdbe | rs587777206 |
MSV3d | rs587777206 |
GWAS Ctlg | rs587777206 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777206(A;A) Rs587777206(G;G) |
Alt | rs587777206(A;A) Rs587777206(G;G) |
Reference | Rs587777206(C;C) |
Significance | Pathogenic |
Disease | Spermatogenic failure 9 |
Variation | info |
Gene | DPY19L2 |
CLNDBN | Spermatogenic failure 9 |
Reversed | 1 |
HGVS | NC_000012.11:g.64017881G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000087745.4, |