rs137854895
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs137854895(-;-) |
Make rs137854895(-;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 74500974 |
Gene | LTBP2 |
is a | snp |
is | mentioned by |
dbSNP | rs137854895 |
dbSNP (classic) | rs137854895 |
ClinGen | rs137854895 |
ebi | rs137854895 |
HLI | rs137854895 |
Exac | rs137854895 |
Gnomad | rs137854895 |
Varsome | rs137854895 |
LitVar | rs137854895 |
Map | rs137854895 |
PheGenI | rs137854895 |
Biobank | rs137854895 |
1000 genomes | rs137854895 |
hgdp | rs137854895 |
ensembl | rs137854895 |
geneview | rs137854895 |
scholar | rs137854895 |
rs137854895 | |
pharmgkb | rs137854895 |
gwascentral | rs137854895 |
openSNP | rs137854895 |
23andMe | rs137854895 |
SNPshot | rs137854895 |
SNPdbe | rs137854895 |
MSV3d | rs137854895 |
GWAS Ctlg | rs137854895 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137854895(-;-) |
Alt | rs137854895(-;-) |
Reference | Rs137854895(C;C) |
Significance | Pathogenic |
Disease | Glaucoma |
Variation | info |
Gene | LTBP2 |
CLNDBN | Glaucoma, congenital |
Reversed | 1 |
HGVS | NC_000014.8:g.74967677delG |
CLNSRC | ClinVar |
CLNACC | RCV000114816.1, |