rs387906786
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs387906786(C;G) |
Make rs387906786(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 34658607 |
Gene | IL11RA |
is a | snp |
is | mentioned by |
dbSNP | rs387906786 |
dbSNP (classic) | rs387906786 |
ClinGen | rs387906786 |
ebi | rs387906786 |
HLI | rs387906786 |
Exac | rs387906786 |
Gnomad | rs387906786 |
Varsome | rs387906786 |
LitVar | rs387906786 |
Map | rs387906786 |
PheGenI | rs387906786 |
Biobank | rs387906786 |
1000 genomes | rs387906786 |
hgdp | rs387906786 |
ensembl | rs387906786 |
geneview | rs387906786 |
scholar | rs387906786 |
rs387906786 | |
pharmgkb | rs387906786 |
gwascentral | rs387906786 |
openSNP | rs387906786 |
23andMe | rs387906786 |
SNPshot | rs387906786 |
SNPdbe | rs387906786 |
MSV3d | rs387906786 |
GWAS Ctlg | rs387906786 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs387906786(G;G) |
Alt | rs387906786(G;G) |
Reference | Rs387906786(C;C) |
Significance | Pathogenic |
Disease | Craniosynostosis and dental anomalies |
Variation | info |
Gene | IL11RA |
CLNDBN | Craniosynostosis and dental anomalies |
Reversed | 0 |
HGVS | NC_000009.11:g.34658604C>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000023049.3, |