rs140984555
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs140984555(C;T) |
Make rs140984555(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 70605421 |
Gene | TEX11 |
is a | snp |
is | mentioned by |
dbSNP | rs140984555 |
dbSNP (classic) | rs140984555 |
ClinGen | rs140984555 |
ebi | rs140984555 |
HLI | rs140984555 |
Exac | rs140984555 |
Gnomad | rs140984555 |
Varsome | rs140984555 |
LitVar | rs140984555 |
Map | rs140984555 |
PheGenI | rs140984555 |
Biobank | rs140984555 |
1000 genomes | rs140984555 |
hgdp | rs140984555 |
ensembl | rs140984555 |
geneview | rs140984555 |
scholar | rs140984555 |
rs140984555 | |
pharmgkb | rs140984555 |
gwascentral | rs140984555 |
openSNP | rs140984555 |
23andMe | rs140984555 |
SNPshot | rs140984555 |
SNPdbe | rs140984555 |
MSV3d | rs140984555 |
GWAS Ctlg | rs140984555 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs140984555(T;T) |
Alt | rs140984555(T;T) |
Reference | Rs140984555(C;C) |
Significance | Pathogenic |
Disease | Spermatogenic failure |
Variation | info |
Gene | TEX11 |
CLNDBN | Spermatogenic failure, X-linked, 2 |
Reversed | 0 |
HGVS | NC_000023.10:g.69825271C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000173009.2, |