rs137854861
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs137854861(C;T) |
Make rs137854861(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 74552291 |
Gene | LTBP2 |
is a | snp |
is | mentioned by |
dbSNP | rs137854861 |
dbSNP (classic) | rs137854861 |
ClinGen | rs137854861 |
ebi | rs137854861 |
HLI | rs137854861 |
Exac | rs137854861 |
Gnomad | rs137854861 |
Varsome | rs137854861 |
LitVar | rs137854861 |
Map | rs137854861 |
PheGenI | rs137854861 |
Biobank | rs137854861 |
1000 genomes | rs137854861 |
hgdp | rs137854861 |
ensembl | rs137854861 |
geneview | rs137854861 |
scholar | rs137854861 |
rs137854861 | |
pharmgkb | rs137854861 |
gwascentral | rs137854861 |
openSNP | rs137854861 |
23andMe | rs137854861 |
SNPshot | rs137854861 |
SNPdbe | rs137854861 |
MSV3d | rs137854861 |
GWAS Ctlg | rs137854861 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137854861(T;T) |
Alt | rs137854861(T;T) |
Reference | Rs137854861(C;C) |
Significance | Probable-Pathogenic |
Disease | Pseudoexfoliation glaucoma |
Variation | info |
Gene | LTBP2 |
CLNDBN | Pseudoexfoliation glaucoma |
Reversed | 1 |
HGVS | NC_000014.8:g.75018994G>A |
CLNSRC | ClinVar |
CLNACC | RCV000114805.1, |