rs1800238
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1800238(G;T) |
Make rs1800238(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 94417738 |
Gene | COL1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs1800238 |
dbSNP (classic) | rs1800238 |
ClinGen | rs1800238 |
ebi | rs1800238 |
HLI | rs1800238 |
Exac | rs1800238 |
Gnomad | rs1800238 |
Varsome | rs1800238 |
LitVar | rs1800238 |
Map | rs1800238 |
PheGenI | rs1800238 |
Biobank | rs1800238 |
1000 genomes | rs1800238 |
hgdp | rs1800238 |
ensembl | rs1800238 |
geneview | rs1800238 |
scholar | rs1800238 |
rs1800238 | |
pharmgkb | rs1800238 |
gwascentral | rs1800238 |
openSNP | rs1800238 |
23andMe | rs1800238 |
SNPshot | rs1800238 |
SNPdbe | rs1800238 |
MSV3d | rs1800238 |
GWAS Ctlg | rs1800238 |
GMAF | 0.1143 |
Max Magnitude | 0 |
[PMID 23800505] Associations of Collagen Type I α2 Polymorphisms with the Presence of Intracranial Aneurysms in Patients from Germany
ClinVar | |
---|---|
Risk | rs1800238(T;T) |
Alt | rs1800238(T;T) |
Reference | Rs1800238(G;G) |
Significance | Non-pathogenic |
Disease | Osteogenesis Imperfecta Ehlers-Danlos syndrome not specified |
Variation | info |
Gene | COL1A2 |
CLNDBN | Osteogenesis Imperfecta, Dominant Ehlers-Danlos syndrome, procollagen proteinase deficient not specified |
Reversed | 0 |
HGVS | NC_000007.13:g.94047050G>T |
CLNSRC | |
CLNACC | RCV000296029.1, RCV000371564.1, RCV000441385.1, |
[PMID 29086084] The association between collagen gene polymorphisms and intracranial aneurysms: a meta-analysis.