rs147088100
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs147088100(A;A) |
Make rs147088100(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 70853248 |
Gene | TEX11 |
is a | snp |
is | mentioned by |
dbSNP | rs147088100 |
dbSNP (classic) | rs147088100 |
ClinGen | rs147088100 |
ebi | rs147088100 |
HLI | rs147088100 |
Exac | rs147088100 |
Gnomad | rs147088100 |
Varsome | rs147088100 |
LitVar | rs147088100 |
Map | rs147088100 |
PheGenI | rs147088100 |
Biobank | rs147088100 |
1000 genomes | rs147088100 |
hgdp | rs147088100 |
ensembl | rs147088100 |
geneview | rs147088100 |
scholar | rs147088100 |
rs147088100 | |
pharmgkb | rs147088100 |
gwascentral | rs147088100 |
openSNP | rs147088100 |
23andMe | rs147088100 |
SNPshot | rs147088100 |
SNPdbe | rs147088100 |
MSV3d | rs147088100 |
GWAS Ctlg | rs147088100 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147088100(A;A) |
Alt | rs147088100(A;A) |
Reference | Rs147088100(G;G) |
Significance | Pathogenic |
Disease | Spermatogenic failure |
Variation | info |
Gene | TEX11 |
CLNDBN | Spermatogenic failure, X-linked, 2 |
Reversed | 0 |
HGVS | NC_000023.10:g.70073098G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000173010.2, |