rs137853866
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs137853866(A;A) |
Make rs137853866(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 64160134 |
Gene | PPIB |
is a | snp |
is | mentioned by |
dbSNP | rs137853866 |
dbSNP (classic) | rs137853866 |
ClinGen | rs137853866 |
ebi | rs137853866 |
HLI | rs137853866 |
Exac | rs137853866 |
Gnomad | rs137853866 |
Varsome | rs137853866 |
LitVar | rs137853866 |
Map | rs137853866 |
PheGenI | rs137853866 |
Biobank | rs137853866 |
1000 genomes | rs137853866 |
hgdp | rs137853866 |
ensembl | rs137853866 |
geneview | rs137853866 |
scholar | rs137853866 |
rs137853866 | |
pharmgkb | rs137853866 |
gwascentral | rs137853866 |
openSNP | rs137853866 |
23andMe | rs137853866 |
SNPshot | rs137853866 |
SNPdbe | rs137853866 |
MSV3d | rs137853866 |
GWAS Ctlg | rs137853866 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137853866(A;A) |
Alt | rs137853866(A;A) |
Reference | Rs137853866(G;G) |
Significance | Pathogenic |
Disease | not provided Osteogenesis imperfecta type 9 |
Variation | info |
Gene | PPIB |
CLNDBN | not provided Osteogenesis imperfecta type 9 |
Reversed | 1 |
HGVS | NC_000015.9:g.64452333C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000024538.1, RCV000202406.1, |