rs769752636
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 5.5 | Ehlers-Danlos Syndrome (EDS) classic type |
Make rs769752636(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 134730386 |
Gene | COL5A1 |
is a | snp |
is | mentioned by |
dbSNP | rs769752636 |
dbSNP (classic) | rs769752636 |
ClinGen | rs769752636 |
ebi | rs769752636 |
HLI | rs769752636 |
Exac | rs769752636 |
Gnomad | rs769752636 |
Varsome | rs769752636 |
LitVar | rs769752636 |
Map | rs769752636 |
PheGenI | rs769752636 |
Biobank | rs769752636 |
1000 genomes | rs769752636 |
hgdp | rs769752636 |
ensembl | rs769752636 |
geneview | rs769752636 |
scholar | rs769752636 |
rs769752636 | |
pharmgkb | rs769752636 |
gwascentral | rs769752636 |
openSNP | rs769752636 |
23andMe | rs769752636 |
SNPshot | rs769752636 |
SNPdbe | rs769752636 |
MSV3d | rs769752636 |
GWAS Ctlg | rs769752636 |
Max Magnitude | 5.5 |
ClinVar | |
---|---|
Risk | rs769752636(A;A) rs769752636(T;T) |
Alt | rs769752636(A;A) rs769752636(T;T) |
Reference | Rs769752636(G;G) |
Significance | Pathogenic |
Disease | Ehlers-Danlos syndrome |
Variation | info |
Gene | COL5A1 |
CLNDBN | Ehlers-Danlos syndrome, classic type |
Reversed | 0 |
HGVS | NC_000009.11:g.137622232G>T |
CLNSRC | |
CLNACC | RCV000467841.1, |