rs111929073
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 6.5 | Ehlers-Danlos Syndrome (EDS) type 4 |
Make rs111929073(A;A) |
Make rs111929073(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 188999471 |
Gene | COL3A1 |
is a | snp |
is | mentioned by |
dbSNP | rs111929073 |
dbSNP (classic) | rs111929073 |
ClinGen | rs111929073 |
ebi | rs111929073 |
HLI | rs111929073 |
Exac | rs111929073 |
Gnomad | rs111929073 |
Varsome | rs111929073 |
LitVar | rs111929073 |
Map | rs111929073 |
PheGenI | rs111929073 |
Biobank | rs111929073 |
1000 genomes | rs111929073 |
hgdp | rs111929073 |
ensembl | rs111929073 |
geneview | rs111929073 |
scholar | rs111929073 |
rs111929073 | |
pharmgkb | rs111929073 |
gwascentral | rs111929073 |
openSNP | rs111929073 |
23andMe | rs111929073 |
SNPshot | rs111929073 |
SNPdbe | rs111929073 |
MSV3d | rs111929073 |
GWAS Ctlg | rs111929073 |
Max Magnitude | 6.5 |
ClinVar | |
---|---|
Risk | rs111929073(A;A) rs111929073(C;C) rs111929073(T;T) |
Alt | rs111929073(A;A) rs111929073(C;C) rs111929073(T;T) |
Reference | Rs111929073(G;G) |
Significance | Other |
Disease | not provided Ehlers-Danlos syndrome |
Variation | info |
Gene | COL3A1 |
CLNDBN | not provided Ehlers-Danlos syndrome, type 4 |
Reversed | 0 |
HGVS | NC_000002.11:g.189864197G>C; NC_000002.11:g.189864197G>T |
CLNSRC | Ehlers-Danlos Syndrome Variant Database COL3A1 |
CLNACC | RCV000434873.1, RCV000087633.2, |