rs869025223
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs869025223(-;-) |
Make rs869025223(-;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 41819588 |
Gene | FKBP10 |
is a | snp |
is | mentioned by |
dbSNP | rs869025223 |
dbSNP (classic) | rs869025223 |
ClinGen | rs869025223 |
ebi | rs869025223 |
HLI | rs869025223 |
Exac | rs869025223 |
Gnomad | rs869025223 |
Varsome | rs869025223 |
LitVar | rs869025223 |
Map | rs869025223 |
PheGenI | rs869025223 |
Biobank | rs869025223 |
1000 genomes | rs869025223 |
hgdp | rs869025223 |
ensembl | rs869025223 |
geneview | rs869025223 |
scholar | rs869025223 |
rs869025223 | |
pharmgkb | rs869025223 |
gwascentral | rs869025223 |
openSNP | rs869025223 |
23andMe | rs869025223 |
SNPshot | rs869025223 |
SNPdbe | rs869025223 |
MSV3d | rs869025223 |
GWAS Ctlg | rs869025223 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs869025223(-;-) |
Alt | rs869025223(-;-) |
Reference | Rs869025223(A;A) |
Significance | Pathogenic |
Disease | Osteogenesis imperfecta |
Variation | info |
Gene | FKBP10 |
CLNDBN | Osteogenesis imperfecta, type XI |
Reversed | 0 |
HGVS | NC_000017.10:g.39975840delA |
CLNSRC | |
CLNACC | RCV000208538.2, |