rs866754647
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs866754647(A;A) |
Make rs866754647(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 83508971 |
Gene | POU3F4 |
is a | snp |
is | mentioned by |
dbSNP | rs866754647 |
dbSNP (classic) | rs866754647 |
ClinGen | rs866754647 |
ebi | rs866754647 |
HLI | rs866754647 |
Exac | rs866754647 |
Gnomad | rs866754647 |
Varsome | rs866754647 |
LitVar | rs866754647 |
Map | rs866754647 |
PheGenI | rs866754647 |
Biobank | rs866754647 |
1000 genomes | rs866754647 |
hgdp | rs866754647 |
ensembl | rs866754647 |
geneview | rs866754647 |
scholar | rs866754647 |
rs866754647 | |
pharmgkb | rs866754647 |
gwascentral | rs866754647 |
openSNP | rs866754647 |
23andMe | rs866754647 |
SNPshot | rs866754647 |
SNPdbe | rs866754647 |
MSV3d | rs866754647 |
GWAS Ctlg | rs866754647 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs866754647(A;A) |
Alt | rs866754647(A;A) |
Reference | Rs866754647(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | POU3F4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.82763979G>A |
CLNSRC | |
CLNACC | RCV000480190.1, |