rs587776910
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587776910(-;G) |
Make rs587776910(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 17 |
Position | 44902471 |
Gene | CCDC103 |
is a | snp |
is | mentioned by |
dbSNP | rs587776910 |
dbSNP (classic) | rs587776910 |
ClinGen | rs587776910 |
ebi | rs587776910 |
HLI | rs587776910 |
Exac | rs587776910 |
Gnomad | rs587776910 |
Varsome | rs587776910 |
LitVar | rs587776910 |
Map | rs587776910 |
PheGenI | rs587776910 |
Biobank | rs587776910 |
1000 genomes | rs587776910 |
hgdp | rs587776910 |
ensembl | rs587776910 |
geneview | rs587776910 |
scholar | rs587776910 |
rs587776910 | |
pharmgkb | rs587776910 |
gwascentral | rs587776910 |
openSNP | rs587776910 |
23andMe | rs587776910 |
SNPshot | rs587776910 |
SNPdbe | rs587776910 |
MSV3d | rs587776910 |
GWAS Ctlg | rs587776910 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776910(G;G) |
Alt | rs587776910(G;G) |
Reference | Rs587776910(-;-) |
Significance | Pathogenic |
Disease | Ciliary dyskinesia Kartagener syndrome |
Variation | info |
Gene | CCDC103 |
CLNDBN | Ciliary dyskinesia, primary, 17 Kartagener syndrome |
Reversed | 0 |
HGVS | NC_000017.10:g.42979839dupG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000024375.4, RCV000190915.1, |