rs886040893
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs886040893(-;-) |
Make rs886040893(-;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 16 |
Position | 50794257 |
Gene | CYLD, LOC105371251 |
is a | snp |
is | mentioned by |
dbSNP | rs886040893 |
dbSNP (classic) | rs886040893 |
ClinGen | rs886040893 |
ebi | rs886040893 |
HLI | rs886040893 |
Exac | rs886040893 |
Gnomad | rs886040893 |
Varsome | rs886040893 |
LitVar | rs886040893 |
Map | rs886040893 |
PheGenI | rs886040893 |
Biobank | rs886040893 |
1000 genomes | rs886040893 |
hgdp | rs886040893 |
ensembl | rs886040893 |
geneview | rs886040893 |
scholar | rs886040893 |
rs886040893 | |
pharmgkb | rs886040893 |
gwascentral | rs886040893 |
openSNP | rs886040893 |
23andMe | rs886040893 |
SNPshot | rs886040893 |
SNPdbe | rs886040893 |
MSV3d | rs886040893 |
GWAS Ctlg | rs886040893 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886040893(-;-) |
Alt | rs886040893(-;-) |
Reference | Rs886040893(T;T) |
Significance | Pathogenic |
Disease | Cylindromatosis |
Variation | info |
Gene | CYLD |
CLNDBN | Cylindromatosis, familial |
Reversed | 0 |
HGVS | NC_000016.9:g.50828168delT |
CLNSRC | |
CLNACC | RCV000257968.1, |