rs200361128
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs200361128(C;G) |
Make rs200361128(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 140504904 |
Gene | SOX3 |
is a | snp |
is | mentioned by |
dbSNP | rs200361128 |
dbSNP (classic) | rs200361128 |
ClinGen | rs200361128 |
ebi | rs200361128 |
HLI | rs200361128 |
Exac | rs200361128 |
Gnomad | rs200361128 |
Varsome | rs200361128 |
LitVar | rs200361128 |
Map | rs200361128 |
PheGenI | rs200361128 |
Biobank | rs200361128 |
1000 genomes | rs200361128 |
hgdp | rs200361128 |
ensembl | rs200361128 |
geneview | rs200361128 |
scholar | rs200361128 |
rs200361128 | |
pharmgkb | rs200361128 |
gwascentral | rs200361128 |
openSNP | rs200361128 |
23andMe | rs200361128 |
SNPshot | rs200361128 |
SNPdbe | rs200361128 |
MSV3d | rs200361128 |
GWAS Ctlg | rs200361128 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200361128(G;G) |
Alt | rs200361128(G;G) |
Reference | Rs200361128(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified Abnormality of brain morphology |
Variation | info |
Gene | SOX3 |
CLNDBN | not specified Abnormality of brain morphology |
Reversed | 0 |
HGVS | NC_000023.10:g.139587069C>G |
CLNSRC | |
CLNACC | RCV000153990.3, RCV000454344.1, |