rs771895449
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AG;AG) | 0 | common in clinvar |
Make rs771895449(-;-) |
Make rs771895449(-;AG) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 8 |
Position | 38145983 |
Gene | STAR |
is a | snp |
is | mentioned by |
dbSNP | rs771895449 |
dbSNP (classic) | rs771895449 |
ClinGen | rs771895449 |
ebi | rs771895449 |
HLI | rs771895449 |
Exac | rs771895449 |
Gnomad | rs771895449 |
Varsome | rs771895449 |
LitVar | rs771895449 |
Map | rs771895449 |
PheGenI | rs771895449 |
Biobank | rs771895449 |
1000 genomes | rs771895449 |
hgdp | rs771895449 |
ensembl | rs771895449 |
geneview | rs771895449 |
scholar | rs771895449 |
rs771895449 | |
pharmgkb | rs771895449 |
gwascentral | rs771895449 |
openSNP | rs771895449 |
23andMe | rs771895449 |
SNPshot | rs771895449 |
SNPdbe | rs771895449 |
MSV3d | rs771895449 |
GWAS Ctlg | rs771895449 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs771895449(-;-) |
Alt | rs771895449(-;-) |
Reference | Rs771895449(AG;AG) |
Significance | Probable-Pathogenic |
Disease | Cholesterol monooxygenase (side-chain cleaving) deficiency |
Variation | info |
Gene | STAR |
CLNDBN | Cholesterol monooxygenase (side-chain cleaving) deficiency |
Reversed | 0 |
HGVS | NC_000008.10:g.38003501_38003502delAG |
CLNSRC | |
CLNACC | RCV000410363.1, |