rs61729440
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs61729440(C;G) |
Make rs61729440(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | X |
Position | 111410133 |
Gene | DCX |
is a | snp |
is | mentioned by |
dbSNP | rs61729440 |
dbSNP (classic) | rs61729440 |
ClinGen | rs61729440 |
ebi | rs61729440 |
HLI | rs61729440 |
Exac | rs61729440 |
Gnomad | rs61729440 |
Varsome | rs61729440 |
LitVar | rs61729440 |
Map | rs61729440 |
PheGenI | rs61729440 |
Biobank | rs61729440 |
1000 genomes | rs61729440 |
hgdp | rs61729440 |
ensembl | rs61729440 |
geneview | rs61729440 |
scholar | rs61729440 |
rs61729440 | |
pharmgkb | rs61729440 |
gwascentral | rs61729440 |
openSNP | rs61729440 |
23andMe | rs61729440 |
SNPshot | rs61729440 |
SNPdbe | rs61729440 |
MSV3d | rs61729440 |
GWAS Ctlg | rs61729440 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs61729440(G;G) |
Alt | rs61729440(G;G) |
Reference | Rs61729440(C;C) |
Significance | Pathogenic |
Disease | Heterotopia |
Variation | info |
Gene | DCX |
CLNDBN | Heterotopia |
Reversed | 0 |
HGVS | NC_000023.10:g.110653361C>G |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000145826.1, |