rs775565634
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs775565634(A;A) |
Make rs775565634(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 53339808 |
Gene | DCC |
is a | snp |
is | mentioned by |
dbSNP | rs775565634 |
dbSNP (classic) | rs775565634 |
ClinGen | rs775565634 |
ebi | rs775565634 |
HLI | rs775565634 |
Exac | rs775565634 |
Gnomad | rs775565634 |
Varsome | rs775565634 |
LitVar | rs775565634 |
Map | rs775565634 |
PheGenI | rs775565634 |
Biobank | rs775565634 |
1000 genomes | rs775565634 |
hgdp | rs775565634 |
ensembl | rs775565634 |
geneview | rs775565634 |
scholar | rs775565634 |
rs775565634 | |
pharmgkb | rs775565634 |
gwascentral | rs775565634 |
openSNP | rs775565634 |
23andMe | rs775565634 |
SNPshot | rs775565634 |
SNPdbe | rs775565634 |
MSV3d | rs775565634 |
GWAS Ctlg | rs775565634 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775565634(A;A) |
Alt | rs775565634(A;A) |
Reference | Rs775565634(G;G) |
Significance | Pathogenic |
Disease | Corpus callosum agenesis |
Variation | info |
Gene | DCC |
CLNDBN | Corpus callosum agenesis |
Reversed | 0 |
HGVS | NC_000018.9:g.50866178G>A |
CLNSRC | |
CLNACC | RCV000416318.1, |