rs587777768
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CG;CG) | 0 | common in clinvar |
Make rs587777768(CG;TA) |
Make rs587777768(TA;TA) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 119030627 |
Gene | NANOS1 |
is a | snp |
is | mentioned by |
dbSNP | rs587777768 |
dbSNP (classic) | rs587777768 |
ClinGen | rs587777768 |
ebi | rs587777768 |
HLI | rs587777768 |
Exac | rs587777768 |
Gnomad | rs587777768 |
Varsome | rs587777768 |
LitVar | rs587777768 |
Map | rs587777768 |
PheGenI | rs587777768 |
Biobank | rs587777768 |
1000 genomes | rs587777768 |
hgdp | rs587777768 |
ensembl | rs587777768 |
geneview | rs587777768 |
scholar | rs587777768 |
rs587777768 | |
pharmgkb | rs587777768 |
gwascentral | rs587777768 |
openSNP | rs587777768 |
23andMe | rs587777768 |
SNPshot | rs587777768 |
SNPdbe | rs587777768 |
MSV3d | rs587777768 |
GWAS Ctlg | rs587777768 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587777768(TA;TA) |
Alt | rs587777768(TA;TA) |
Reference | Rs587777768(CG;CG) |
Significance | Pathogenic |
Disease | Spermatogenic failure 12 |
Variation | info |
Gene | NANOS1 |
CLNDBN | Spermatogenic failure 12 |
Reversed | 0 |
HGVS | NC_000010.10:g.120790139_120790140delCGinsTA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000055619.2, |