rs766029215
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs766029215(A;A) |
Make rs766029215(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 62821531 |
Gene | COL9A3 |
is a | snp |
is | mentioned by |
dbSNP | rs766029215 |
dbSNP (classic) | rs766029215 |
ClinGen | rs766029215 |
ebi | rs766029215 |
HLI | rs766029215 |
Exac | rs766029215 |
Gnomad | rs766029215 |
Varsome | rs766029215 |
LitVar | rs766029215 |
Map | rs766029215 |
PheGenI | rs766029215 |
Biobank | rs766029215 |
1000 genomes | rs766029215 |
hgdp | rs766029215 |
ensembl | rs766029215 |
geneview | rs766029215 |
scholar | rs766029215 |
rs766029215 | |
pharmgkb | rs766029215 |
gwascentral | rs766029215 |
openSNP | rs766029215 |
23andMe | rs766029215 |
SNPshot | rs766029215 |
SNPdbe | rs766029215 |
MSV3d | rs766029215 |
GWAS Ctlg | rs766029215 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs766029215(A;A) |
Alt | rs766029215(A;A) |
Reference | Rs766029215(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | COL9A3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.61452883G>A |
CLNSRC | |
CLNACC | RCV000413769.1, |