rs796052239
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CATGTGG;CATGTGG) | 0 | common in clinvar |
Make rs796052239(-;-) |
Make rs796052239(-;TGTGGCA) |
Make rs796052239(TGTGGCA;TGTGGCA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 41334261 |
Gene | DDX3X, LOC105373184, LOC107985678 |
is a | snp |
is | mentioned by |
dbSNP | rs796052239 |
dbSNP (classic) | rs796052239 |
ClinGen | rs796052239 |
ebi | rs796052239 |
HLI | rs796052239 |
Exac | rs796052239 |
Gnomad | rs796052239 |
Varsome | rs796052239 |
LitVar | rs796052239 |
Map | rs796052239 |
PheGenI | rs796052239 |
Biobank | rs796052239 |
1000 genomes | rs796052239 |
hgdp | rs796052239 |
ensembl | rs796052239 |
geneview | rs796052239 |
scholar | rs796052239 |
rs796052239 | |
pharmgkb | rs796052239 |
gwascentral | rs796052239 |
openSNP | rs796052239 |
23andMe | rs796052239 |
SNPshot | rs796052239 |
SNPdbe | rs796052239 |
MSV3d | rs796052239 |
GWAS Ctlg | rs796052239 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs796052239(CATGTGG;CATGTGG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DDX3X |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.41193514_41193520delTGTGGCA |
CLNSRC | |
CLNACC | RCV000190116.1, |