rs797044889
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(CG;CG) | 0 | common in clinvar |
Make rs797044889(-;-) |
Make rs797044889(-;CG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 53250523 |
Gene | IQSEC2 |
is a | snp |
is | mentioned by |
dbSNP | rs797044889 |
dbSNP (classic) | rs797044889 |
ClinGen | rs797044889 |
ebi | rs797044889 |
HLI | rs797044889 |
Exac | rs797044889 |
Gnomad | rs797044889 |
Varsome | rs797044889 |
LitVar | rs797044889 |
Map | rs797044889 |
PheGenI | rs797044889 |
Biobank | rs797044889 |
1000 genomes | rs797044889 |
hgdp | rs797044889 |
ensembl | rs797044889 |
geneview | rs797044889 |
scholar | rs797044889 |
rs797044889 | |
pharmgkb | rs797044889 |
gwascentral | rs797044889 |
openSNP | rs797044889 |
23andMe | rs797044889 |
SNPshot | rs797044889 |
SNPdbe | rs797044889 |
MSV3d | rs797044889 |
GWAS Ctlg | rs797044889 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044889(-;-) |
Alt | rs797044889(-;-) |
Reference | Rs797044889(CG;CG) |
Significance | Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | IQSEC2 |
CLNDBN | Inborn genetic diseases |
Reversed | 1 |
HGVS | NC_000023.10:g.53279705_53279706delCG |
CLNSRC | |
CLNACC | RCV000190711.1, |