rs770285398
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TTGT;TTGT) | 0 | common in clinvar |
Make rs770285398(-;-) |
Make rs770285398(-;TTGT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 8 |
Position | 64616217 |
Gene | CYP7B1 |
is a | snp |
is | mentioned by |
dbSNP | rs770285398 |
dbSNP (classic) | rs770285398 |
ClinGen | rs770285398 |
ebi | rs770285398 |
HLI | rs770285398 |
Exac | rs770285398 |
Gnomad | rs770285398 |
Varsome | rs770285398 |
LitVar | rs770285398 |
Map | rs770285398 |
PheGenI | rs770285398 |
Biobank | rs770285398 |
1000 genomes | rs770285398 |
hgdp | rs770285398 |
ensembl | rs770285398 |
geneview | rs770285398 |
scholar | rs770285398 |
rs770285398 | |
pharmgkb | rs770285398 |
gwascentral | rs770285398 |
openSNP | rs770285398 |
23andMe | rs770285398 |
SNPshot | rs770285398 |
SNPdbe | rs770285398 |
MSV3d | rs770285398 |
GWAS Ctlg | rs770285398 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs770285398(-;-) |
Alt | rs770285398(-;-) |
Reference | Rs770285398(TTGT;TTGT) |
Significance | Pathogenic |
Disease | Spastic paraplegia |
Variation | info |
Gene | CYP7B1 |
CLNDBN | Spastic paraplegia |
Reversed | 0 |
HGVS | NC_000008.10:g.65528774_65528777delTTGT |
CLNSRC | |
CLNACC | RCV000227207.1, |