rs121909082
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs121909082(A;A) |
Make rs121909082(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 91724229 |
Gene | ROR2 |
is a | snp |
is | mentioned by |
dbSNP | rs121909082 |
dbSNP (classic) | rs121909082 |
ClinGen | rs121909082 |
ebi | rs121909082 |
HLI | rs121909082 |
Exac | rs121909082 |
Gnomad | rs121909082 |
Varsome | rs121909082 |
LitVar | rs121909082 |
Map | rs121909082 |
PheGenI | rs121909082 |
Biobank | rs121909082 |
1000 genomes | rs121909082 |
hgdp | rs121909082 |
ensembl | rs121909082 |
geneview | rs121909082 |
scholar | rs121909082 |
rs121909082 | |
pharmgkb | rs121909082 |
gwascentral | rs121909082 |
openSNP | rs121909082 |
23andMe | rs121909082 |
SNPshot | rs121909082 |
SNPdbe | rs121909082 |
MSV3d | rs121909082 |
GWAS Ctlg | rs121909082 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909082(A;A) rs121909082(T;T) |
Alt | rs121909082(A;A) rs121909082(T;T) |
Reference | Rs121909082(C;C) |
Significance | Pathogenic |
Disease | Brachydactyly type B1 |
Variation | info |
Gene | ROR2 |
CLNDBN | Brachydactyly type B1 |
Reversed | 1 |
HGVS | NC_000009.11:g.94486511G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000007727.3, |