rs876657647
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs876657647(G;G) |
Make rs876657647(G;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 90759569 |
Gene | ADGRV1 |
is a | snp |
is | mentioned by |
dbSNP | rs876657647 |
dbSNP (classic) | rs876657647 |
ClinGen | rs876657647 |
ebi | rs876657647 |
HLI | rs876657647 |
Exac | rs876657647 |
Gnomad | rs876657647 |
Varsome | rs876657647 |
LitVar | rs876657647 |
Map | rs876657647 |
PheGenI | rs876657647 |
Biobank | rs876657647 |
1000 genomes | rs876657647 |
hgdp | rs876657647 |
ensembl | rs876657647 |
geneview | rs876657647 |
scholar | rs876657647 |
rs876657647 | |
pharmgkb | rs876657647 |
gwascentral | rs876657647 |
openSNP | rs876657647 |
23andMe | rs876657647 |
SNPshot | rs876657647 |
SNPdbe | rs876657647 |
MSV3d | rs876657647 |
GWAS Ctlg | rs876657647 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876657647(G;G) |
Alt | rs876657647(G;G) |
Reference | Rs876657647(T;T) |
Significance | Probable-Pathogenic |
Disease | Usher syndrome |
Variation | info |
Gene | GPR98 ADGRV1 |
CLNDBN | Usher syndrome, type 2C |
Reversed | 0 |
HGVS | NC_000005.9:g.90055386T>G |
CLNSRC | |
CLNACC | RCV000221151.1, |