rs369432845
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs369432845(G;T) |
Make rs369432845(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 40062275 |
Gene | BCOR |
is a | snp |
is | mentioned by |
dbSNP | rs369432845 |
dbSNP (classic) | rs369432845 |
ClinGen | rs369432845 |
ebi | rs369432845 |
HLI | rs369432845 |
Exac | rs369432845 |
Gnomad | rs369432845 |
Varsome | rs369432845 |
LitVar | rs369432845 |
Map | rs369432845 |
PheGenI | rs369432845 |
Biobank | rs369432845 |
1000 genomes | rs369432845 |
hgdp | rs369432845 |
ensembl | rs369432845 |
geneview | rs369432845 |
scholar | rs369432845 |
rs369432845 | |
pharmgkb | rs369432845 |
gwascentral | rs369432845 |
openSNP | rs369432845 |
23andMe | rs369432845 |
SNPshot | rs369432845 |
SNPdbe | rs369432845 |
MSV3d | rs369432845 |
GWAS Ctlg | rs369432845 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369432845(A;A) rs369432845(T;T) |
Alt | rs369432845(A;A) rs369432845(T;T) |
Reference | Rs369432845(G;G) |
Significance | Probable-Pathogenic |
Disease | Abnormality of brain morphology |
Variation | info |
Gene | BCOR |
CLNDBN | Abnormality of brain morphology |
Reversed | 0 |
HGVS | NC_000023.10:g.39921528G>T |
CLNSRC | |
CLNACC | RCV000454264.1, |