rs150231967
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs150231967(A;A) |
Make rs150231967(A;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 10 |
Position | 49750849 |
Gene | OGDHL |
is a | snp |
is | mentioned by |
dbSNP | rs150231967 |
dbSNP (classic) | rs150231967 |
ClinGen | rs150231967 |
ebi | rs150231967 |
HLI | rs150231967 |
Exac | rs150231967 |
Gnomad | rs150231967 |
Varsome | rs150231967 |
LitVar | rs150231967 |
Map | rs150231967 |
PheGenI | rs150231967 |
Biobank | rs150231967 |
1000 genomes | rs150231967 |
hgdp | rs150231967 |
ensembl | rs150231967 |
geneview | rs150231967 |
scholar | rs150231967 |
rs150231967 | |
pharmgkb | rs150231967 |
gwascentral | rs150231967 |
openSNP | rs150231967 |
23andMe | rs150231967 |
SNPshot | rs150231967 |
SNPdbe | rs150231967 |
MSV3d | rs150231967 |
GWAS Ctlg | rs150231967 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs150231967(A;A) |
Alt | rs150231967(A;A) |
Reference | Rs150231967(T;T) |
Significance | Probable-Pathogenic |
Disease | Inborn genetic diseases |
Variation | info |
Gene | OGDHL |
CLNDBN | Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000010.10:g.50958895T>A |
CLNSRC | |
CLNACC | RCV000210590.1, |