rs773726323
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs773726323(C;T) |
Make rs773726323(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 2 |
Position | 189062882 |
Gene | COL5A2 |
is a | snp |
is | mentioned by |
dbSNP | rs773726323 |
dbSNP (classic) | rs773726323 |
ClinGen | rs773726323 |
ebi | rs773726323 |
HLI | rs773726323 |
Exac | rs773726323 |
Gnomad | rs773726323 |
Varsome | rs773726323 |
LitVar | rs773726323 |
Map | rs773726323 |
PheGenI | rs773726323 |
Biobank | rs773726323 |
1000 genomes | rs773726323 |
hgdp | rs773726323 |
ensembl | rs773726323 |
geneview | rs773726323 |
scholar | rs773726323 |
rs773726323 | |
pharmgkb | rs773726323 |
gwascentral | rs773726323 |
openSNP | rs773726323 |
23andMe | rs773726323 |
SNPshot | rs773726323 |
SNPdbe | rs773726323 |
MSV3d | rs773726323 |
GWAS Ctlg | rs773726323 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773726323(T;T) |
Alt | rs773726323(T;T) |
Reference | Rs773726323(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | COL5A2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.189927608C>T |
CLNSRC | |
CLNACC | RCV000200772.1, |