rs767570081
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs767570081(C;T) |
Make rs767570081(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 90755015 |
Gene | ADGRV1 |
is a | snp |
is | mentioned by |
dbSNP | rs767570081 |
dbSNP (classic) | rs767570081 |
ClinGen | rs767570081 |
ebi | rs767570081 |
HLI | rs767570081 |
Exac | rs767570081 |
Gnomad | rs767570081 |
Varsome | rs767570081 |
LitVar | rs767570081 |
Map | rs767570081 |
PheGenI | rs767570081 |
Biobank | rs767570081 |
1000 genomes | rs767570081 |
hgdp | rs767570081 |
ensembl | rs767570081 |
geneview | rs767570081 |
scholar | rs767570081 |
rs767570081 | |
pharmgkb | rs767570081 |
gwascentral | rs767570081 |
openSNP | rs767570081 |
23andMe | rs767570081 |
SNPshot | rs767570081 |
SNPdbe | rs767570081 |
MSV3d | rs767570081 |
GWAS Ctlg | rs767570081 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs767570081(T;T) |
Alt | rs767570081(T;T) |
Reference | Rs767570081(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GPR98 ADGRV1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.90050832C>T |
CLNSRC | |
CLNACC | RCV000413951.1, |