rs748112308
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs748112308(A;A) |
Make rs748112308(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 53486808 |
Gene | DCC |
is a | snp |
is | mentioned by |
dbSNP | rs748112308 |
dbSNP (classic) | rs748112308 |
ClinGen | rs748112308 |
ebi | rs748112308 |
HLI | rs748112308 |
Exac | rs748112308 |
Gnomad | rs748112308 |
Varsome | rs748112308 |
LitVar | rs748112308 |
Map | rs748112308 |
PheGenI | rs748112308 |
Biobank | rs748112308 |
1000 genomes | rs748112308 |
hgdp | rs748112308 |
ensembl | rs748112308 |
geneview | rs748112308 |
scholar | rs748112308 |
rs748112308 | |
pharmgkb | rs748112308 |
gwascentral | rs748112308 |
openSNP | rs748112308 |
23andMe | rs748112308 |
SNPshot | rs748112308 |
SNPdbe | rs748112308 |
MSV3d | rs748112308 |
GWAS Ctlg | rs748112308 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748112308(A;A) |
Alt | rs748112308(A;A) |
Reference | Rs748112308(G;G) |
Significance | Pathogenic |
Disease | Corpus callosum agenesis |
Variation | info |
Gene | DCC |
CLNDBN | Corpus callosum agenesis |
Reversed | 0 |
HGVS | NC_000018.9:g.51013178G>A |
CLNSRC | |
CLNACC | RCV000416369.1, |