rs796052229
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs796052229(-;TA) |
Make rs796052229(TA;TA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 41346298 |
Gene | DDX3X |
is a | snp |
is | mentioned by |
dbSNP | rs796052229 |
dbSNP (classic) | rs796052229 |
ClinGen | rs796052229 |
ebi | rs796052229 |
HLI | rs796052229 |
Exac | rs796052229 |
Gnomad | rs796052229 |
Varsome | rs796052229 |
LitVar | rs796052229 |
Map | rs796052229 |
PheGenI | rs796052229 |
Biobank | rs796052229 |
1000 genomes | rs796052229 |
hgdp | rs796052229 |
ensembl | rs796052229 |
geneview | rs796052229 |
scholar | rs796052229 |
rs796052229 | |
pharmgkb | rs796052229 |
gwascentral | rs796052229 |
openSNP | rs796052229 |
23andMe | rs796052229 |
SNPshot | rs796052229 |
SNPdbe | rs796052229 |
MSV3d | rs796052229 |
GWAS Ctlg | rs796052229 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796052229(TA;TA) |
Alt | rs796052229(TA;TA) |
Reference | Rs796052229(;) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DDX3X |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.41205550_41205551dupTA |
CLNSRC | |
CLNACC | RCV000190106.1, |