rs371981035
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs371981035(A;G) |
Make rs371981035(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 90810231 |
Gene | ADGRV1 |
is a | snp |
is | mentioned by |
dbSNP | rs371981035 |
dbSNP (classic) | rs371981035 |
ClinGen | rs371981035 |
ebi | rs371981035 |
HLI | rs371981035 |
Exac | rs371981035 |
Gnomad | rs371981035 |
Varsome | rs371981035 |
LitVar | rs371981035 |
Map | rs371981035 |
PheGenI | rs371981035 |
Biobank | rs371981035 |
1000 genomes | rs371981035 |
hgdp | rs371981035 |
ensembl | rs371981035 |
geneview | rs371981035 |
scholar | rs371981035 |
rs371981035 | |
pharmgkb | rs371981035 |
gwascentral | rs371981035 |
openSNP | rs371981035 |
23andMe | rs371981035 |
SNPshot | rs371981035 |
SNPdbe | rs371981035 |
MSV3d | rs371981035 |
GWAS Ctlg | rs371981035 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs371981035(G;G) |
Alt | rs371981035(G;G) |
Reference | Rs371981035(A;A) |
Significance | Pathogenic |
Disease | Usher syndrome |
Variation | info |
Gene | ADGRV1 GPR98 |
CLNDBN | Usher syndrome, type 2C |
Reversed | 0 |
HGVS | NC_000005.9:g.90106048A>G |
CLNSRC | ClinVar |
CLNACC | RCV000039531.2, |