rs777425801
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs777425801(C;T) |
Make rs777425801(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 71441413 |
Gene | DHCR7 |
is a | snp |
is | mentioned by |
dbSNP | rs777425801 |
dbSNP (classic) | rs777425801 |
ClinGen | rs777425801 |
ebi | rs777425801 |
HLI | rs777425801 |
Exac | rs777425801 |
Gnomad | rs777425801 |
Varsome | rs777425801 |
LitVar | rs777425801 |
Map | rs777425801 |
PheGenI | rs777425801 |
Biobank | rs777425801 |
1000 genomes | rs777425801 |
hgdp | rs777425801 |
ensembl | rs777425801 |
geneview | rs777425801 |
scholar | rs777425801 |
rs777425801 | |
pharmgkb | rs777425801 |
gwascentral | rs777425801 |
openSNP | rs777425801 |
23andMe | rs777425801 |
SNPshot | rs777425801 |
SNPdbe | rs777425801 |
MSV3d | rs777425801 |
GWAS Ctlg | rs777425801 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs777425801(T;T) |
Alt | rs777425801(T;T) |
Reference | Rs777425801(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DHCR7 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.71152459C>T |
CLNSRC | |
CLNACC | RCV000421810.1, |