rs794729172
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CG;CG) | 0 | common in clinvar |
Make rs794729172(A;A) |
Make rs794729172(A;CG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 154420705 |
Gene | TAZ |
is a | snp |
is | mentioned by |
dbSNP | rs794729172 |
dbSNP (classic) | rs794729172 |
ClinGen | rs794729172 |
ebi | rs794729172 |
HLI | rs794729172 |
Exac | rs794729172 |
Gnomad | rs794729172 |
Varsome | rs794729172 |
LitVar | rs794729172 |
Map | rs794729172 |
PheGenI | rs794729172 |
Biobank | rs794729172 |
1000 genomes | rs794729172 |
hgdp | rs794729172 |
ensembl | rs794729172 |
geneview | rs794729172 |
scholar | rs794729172 |
rs794729172 | |
pharmgkb | rs794729172 |
gwascentral | rs794729172 |
openSNP | rs794729172 |
23andMe | rs794729172 |
SNPshot | rs794729172 |
SNPdbe | rs794729172 |
MSV3d | rs794729172 |
GWAS Ctlg | rs794729172 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs794729172(A;A) |
Alt | rs794729172(A;A) |
Reference | Rs794729172(CG;CG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TAZ |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.153649044_153649045delCGinsA |
CLNSRC | |
CLNACC | RCV000183913.1, |