rs773888308
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs773888308(A;A) |
Make rs773888308(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 10 |
Position | 49738249 |
Gene | OGDHL |
is a | snp |
is | mentioned by |
dbSNP | rs773888308 |
dbSNP (classic) | rs773888308 |
ClinGen | rs773888308 |
ebi | rs773888308 |
HLI | rs773888308 |
Exac | rs773888308 |
Gnomad | rs773888308 |
Varsome | rs773888308 |
LitVar | rs773888308 |
Map | rs773888308 |
PheGenI | rs773888308 |
Biobank | rs773888308 |
1000 genomes | rs773888308 |
hgdp | rs773888308 |
ensembl | rs773888308 |
geneview | rs773888308 |
scholar | rs773888308 |
rs773888308 | |
pharmgkb | rs773888308 |
gwascentral | rs773888308 |
openSNP | rs773888308 |
23andMe | rs773888308 |
SNPshot | rs773888308 |
SNPdbe | rs773888308 |
MSV3d | rs773888308 |
GWAS Ctlg | rs773888308 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773888308(A;A) |
Alt | rs773888308(A;A) |
Reference | Rs773888308(G;G) |
Significance | Probable-Pathogenic |
Disease | Abnormality of brain morphology |
Variation | info |
Gene | OGDHL |
CLNDBN | Abnormality of brain morphology |
Reversed | 0 |
HGVS | NC_000010.10:g.50946295G>A |
CLNSRC | |
CLNACC | RCV000454186.1, |