rs730882190
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs730882190(-;G) |
Make rs730882190(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 103006072 |
Gene | COL11A1 |
is a | snp |
is | mentioned by |
dbSNP | rs730882190 |
dbSNP (classic) | rs730882190 |
ClinGen | rs730882190 |
ebi | rs730882190 |
HLI | rs730882190 |
Exac | rs730882190 |
Gnomad | rs730882190 |
Varsome | rs730882190 |
LitVar | rs730882190 |
Map | rs730882190 |
PheGenI | rs730882190 |
Biobank | rs730882190 |
1000 genomes | rs730882190 |
hgdp | rs730882190 |
ensembl | rs730882190 |
geneview | rs730882190 |
scholar | rs730882190 |
rs730882190 | |
pharmgkb | rs730882190 |
gwascentral | rs730882190 |
openSNP | rs730882190 |
23andMe | rs730882190 |
SNPshot | rs730882190 |
SNPdbe | rs730882190 |
MSV3d | rs730882190 |
GWAS Ctlg | rs730882190 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730882190(G;G) |
Alt | rs730882190(G;G) |
Reference | Rs730882190(-;-) |
Significance | Pathogenic |
Disease | Fibrochondrogenesis |
Variation | info |
Gene | COL11A1 |
CLNDBN | Fibrochondrogenesis |
Reversed | 1 |
HGVS | NC_000001.10:g.103471629dupC |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000022494.29, |