rs189754995
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs189754995(G;T) |
Make rs189754995(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 70255375 |
Gene | COL9A1 |
is a | snp |
is | mentioned by |
dbSNP | rs189754995 |
dbSNP (classic) | rs189754995 |
ClinGen | rs189754995 |
ebi | rs189754995 |
HLI | rs189754995 |
Exac | rs189754995 |
Gnomad | rs189754995 |
Varsome | rs189754995 |
LitVar | rs189754995 |
Map | rs189754995 |
PheGenI | rs189754995 |
Biobank | rs189754995 |
1000 genomes | rs189754995 |
hgdp | rs189754995 |
ensembl | rs189754995 |
geneview | rs189754995 |
scholar | rs189754995 |
rs189754995 | |
pharmgkb | rs189754995 |
gwascentral | rs189754995 |
openSNP | rs189754995 |
23andMe | rs189754995 |
SNPshot | rs189754995 |
SNPdbe | rs189754995 |
MSV3d | rs189754995 |
GWAS Ctlg | rs189754995 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs189754995(A;A) rs189754995(T;T) |
Alt | rs189754995(A;A) rs189754995(T;T) |
Reference | Rs189754995(G;G) |
Significance | Pathogenic |
Disease | Stickler syndrome |
Variation | info |
Gene | COL9A1 |
CLNDBN | Stickler syndrome, type 4 |
Reversed | 0 |
HGVS | NC_000006.11:g.70965078G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000148951.2, |