rs797044723
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AT;AT) | 0 | common in clinvar |
Make rs797044723(-;-) |
Make rs797044723(-;AT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 77508463 |
Gene | ATRX |
is a | snp |
is | mentioned by |
dbSNP | rs797044723 |
dbSNP (classic) | rs797044723 |
ClinGen | rs797044723 |
ebi | rs797044723 |
HLI | rs797044723 |
Exac | rs797044723 |
Gnomad | rs797044723 |
Varsome | rs797044723 |
LitVar | rs797044723 |
Map | rs797044723 |
PheGenI | rs797044723 |
Biobank | rs797044723 |
1000 genomes | rs797044723 |
hgdp | rs797044723 |
ensembl | rs797044723 |
geneview | rs797044723 |
scholar | rs797044723 |
rs797044723 | |
pharmgkb | rs797044723 |
gwascentral | rs797044723 |
openSNP | rs797044723 |
23andMe | rs797044723 |
SNPshot | rs797044723 |
SNPdbe | rs797044723 |
MSV3d | rs797044723 |
GWAS Ctlg | rs797044723 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044723(-;-) |
Alt | rs797044723(-;-) |
Reference | Rs797044723(AT;AT) |
Significance | Pathogenic |
Disease | ATR-X syndrome not provided |
Variation | info |
Gene | ATRX |
CLNDBN | ATR-X syndrome not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.76763941_76763942delAT |
CLNSRC | |
CLNACC | RCV000177828.1, RCV000316314.1, |