rs763670293
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs763670293(C;T) |
Make rs763670293(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 5 |
Position | 90728720 |
Gene | ADGRV1, LOC105379077 |
is a | snp |
is | mentioned by |
dbSNP | rs763670293 |
dbSNP (classic) | rs763670293 |
ClinGen | rs763670293 |
ebi | rs763670293 |
HLI | rs763670293 |
Exac | rs763670293 |
Gnomad | rs763670293 |
Varsome | rs763670293 |
LitVar | rs763670293 |
Map | rs763670293 |
PheGenI | rs763670293 |
Biobank | rs763670293 |
1000 genomes | rs763670293 |
hgdp | rs763670293 |
ensembl | rs763670293 |
geneview | rs763670293 |
scholar | rs763670293 |
rs763670293 | |
pharmgkb | rs763670293 |
gwascentral | rs763670293 |
openSNP | rs763670293 |
23andMe | rs763670293 |
SNPshot | rs763670293 |
SNPdbe | rs763670293 |
MSV3d | rs763670293 |
GWAS Ctlg | rs763670293 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763670293(T;T) |
Alt | rs763670293(T;T) |
Reference | Rs763670293(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADGRV1 GPR98 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.90024537C>T |
CLNSRC | |
CLNACC | RCV000255292.1, |