rs727504777
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs727504777(C;T) |
Make rs727504777(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 90778008 |
Gene | ADGRV1 |
is a | snp |
is | mentioned by |
dbSNP | rs727504777 |
dbSNP (classic) | rs727504777 |
ClinGen | rs727504777 |
ebi | rs727504777 |
HLI | rs727504777 |
Exac | rs727504777 |
Gnomad | rs727504777 |
Varsome | rs727504777 |
LitVar | rs727504777 |
Map | rs727504777 |
PheGenI | rs727504777 |
Biobank | rs727504777 |
1000 genomes | rs727504777 |
hgdp | rs727504777 |
ensembl | rs727504777 |
geneview | rs727504777 |
scholar | rs727504777 |
rs727504777 | |
pharmgkb | rs727504777 |
gwascentral | rs727504777 |
openSNP | rs727504777 |
23andMe | rs727504777 |
SNPshot | rs727504777 |
SNPdbe | rs727504777 |
MSV3d | rs727504777 |
GWAS Ctlg | rs727504777 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs727504777(T;T) |
Alt | rs727504777(T;T) |
Reference | Rs727504777(C;C) |
Significance | Pathogenic |
Disease | Usher syndrome |
Variation | info |
Gene | GPR98 ADGRV1 |
CLNDBN | Usher syndrome, type 2C |
Reversed | 0 |
HGVS | NC_000005.9:g.90073825C>T |
CLNSRC | |
CLNACC | RCV000156094.1, |