rs904944428
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs904944428(-;T) |
Make rs904944428(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 6 |
Position | 24301742 |
Gene | DCDC2 |
is a | snp |
is | mentioned by |
dbSNP | rs904944428 |
dbSNP (classic) | rs904944428 |
ClinGen | rs904944428 |
ebi | rs904944428 |
HLI | rs904944428 |
Exac | rs904944428 |
Gnomad | rs904944428 |
Varsome | rs904944428 |
LitVar | rs904944428 |
Map | rs904944428 |
PheGenI | rs904944428 |
Biobank | rs904944428 |
1000 genomes | rs904944428 |
hgdp | rs904944428 |
ensembl | rs904944428 |
geneview | rs904944428 |
scholar | rs904944428 |
rs904944428 | |
pharmgkb | rs904944428 |
gwascentral | rs904944428 |
openSNP | rs904944428 |
23andMe | rs904944428 |
SNPshot | rs904944428 |
SNPdbe | rs904944428 |
MSV3d | rs904944428 |
GWAS Ctlg | rs904944428 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs904944428(T;T) |
Alt | rs904944428(T;T) |
Reference | Rs904944428(-;-) |
Significance | Pathogenic |
Disease | Sclerosing cholangitis |
Variation | info |
Gene | DCDC2 |
CLNDBN | Sclerosing cholangitis, neonatal |
Reversed | 0 |
HGVS | NC_000006.11:g.24301971dup |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000477740.1, |