rs764193290
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs764193290(-;-) |
Make rs764193290(-;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 237342163 |
Gene | COL6A3 |
is a | snp |
is | mentioned by |
dbSNP | rs764193290 |
dbSNP (classic) | rs764193290 |
ClinGen | rs764193290 |
ebi | rs764193290 |
HLI | rs764193290 |
Exac | rs764193290 |
Gnomad | rs764193290 |
Varsome | rs764193290 |
LitVar | rs764193290 |
Map | rs764193290 |
PheGenI | rs764193290 |
Biobank | rs764193290 |
1000 genomes | rs764193290 |
hgdp | rs764193290 |
ensembl | rs764193290 |
geneview | rs764193290 |
scholar | rs764193290 |
rs764193290 | |
pharmgkb | rs764193290 |
gwascentral | rs764193290 |
openSNP | rs764193290 |
23andMe | rs764193290 |
SNPshot | rs764193290 |
SNPdbe | rs764193290 |
MSV3d | rs764193290 |
GWAS Ctlg | rs764193290 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs764193290(-;-) |
Alt | rs764193290(-;-) |
Reference | Rs764193290(T;T) |
Significance | Probable-Pathogenic |
Disease | Bethlem myopathy 1 Dystonia 27 Ullrich congenital muscular dystrophy 1 |
Variation | info |
Gene | COL6A3 |
CLNDBN | Bethlem myopathy 1 Dystonia 27 Ullrich congenital muscular dystrophy 1 |
Reversed | 0 |
HGVS | NC_000002.11:g.238250806delT |
CLNSRC | |
CLNACC | RCV000477801.1, |