rs387907325
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs387907325(-;T) |
Make rs387907325(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 41819560 |
Gene | FKBP10 |
is a | snp |
is | mentioned by |
dbSNP | rs387907325 |
dbSNP (classic) | rs387907325 |
ClinGen | rs387907325 |
ebi | rs387907325 |
HLI | rs387907325 |
Exac | rs387907325 |
Gnomad | rs387907325 |
Varsome | rs387907325 |
LitVar | rs387907325 |
Map | rs387907325 |
PheGenI | rs387907325 |
Biobank | rs387907325 |
1000 genomes | rs387907325 |
hgdp | rs387907325 |
ensembl | rs387907325 |
geneview | rs387907325 |
scholar | rs387907325 |
rs387907325 | |
pharmgkb | rs387907325 |
gwascentral | rs387907325 |
openSNP | rs387907325 |
23andMe | rs387907325 |
SNPshot | rs387907325 |
SNPdbe | rs387907325 |
MSV3d | rs387907325 |
GWAS Ctlg | rs387907325 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387907325(T;T) |
Alt | rs387907325(T;T) |
Reference | Rs387907325(-;-) |
Significance | Pathogenic |
Disease | Osteogenesis imperfecta type 12 |
Variation | info |
Gene | FKBP10 |
CLNDBN | Osteogenesis imperfecta type 12 |
Reversed | 0 |
HGVS | NC_000017.10:g.39975812dupT |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000034825.7, |