rs72659345
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAAT;AAAT) | 0 | common in clinvar |
(ATAA;ATAA) | 0 | common in clinvar |
(I;I) | 0 |
Make rs72659345(-;-) |
Make rs72659345(-;ATAA) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 94430293 |
Gene | COL1A2 |
is a | snp |
is | mentioned by |
dbSNP | rs72659345 |
dbSNP (classic) | rs72659345 |
ClinGen | rs72659345 |
ebi | rs72659345 |
HLI | rs72659345 |
Exac | rs72659345 |
Gnomad | rs72659345 |
Varsome | rs72659345 |
LitVar | rs72659345 |
Map | rs72659345 |
PheGenI | rs72659345 |
Biobank | rs72659345 |
1000 genomes | rs72659345 |
hgdp | rs72659345 |
ensembl | rs72659345 |
geneview | rs72659345 |
scholar | rs72659345 |
rs72659345 | |
pharmgkb | rs72659345 |
gwascentral | rs72659345 |
openSNP | rs72659345 |
23andMe | rs72659345 |
SNPshot | rs72659345 |
SNPdbe | rs72659345 |
MSV3d | rs72659345 |
GWAS Ctlg | rs72659345 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs72659345(-;-) |
Alt | rs72659345(-;-) |
Reference | Rs72659345(AAAT;AAAT) |
Significance | Pathogenic |
Disease | Osteogenesis imperfecta type III |
Variation | info |
Gene | COL1A2 |
CLNDBN | Osteogenesis imperfecta type III |
Reversed | 0 |
HGVS | NC_000007.13:g.94059605_94059608delATAA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000018776.23, |