rs778947880
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs778947880(C;T) |
Make rs778947880(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 18 |
Position | 21765807 |
Gene | MIB1 |
is a | snp |
is | mentioned by |
dbSNP | rs778947880 |
dbSNP (classic) | rs778947880 |
ClinGen | rs778947880 |
ebi | rs778947880 |
HLI | rs778947880 |
Exac | rs778947880 |
Gnomad | rs778947880 |
Varsome | rs778947880 |
LitVar | rs778947880 |
Map | rs778947880 |
PheGenI | rs778947880 |
Biobank | rs778947880 |
1000 genomes | rs778947880 |
hgdp | rs778947880 |
ensembl | rs778947880 |
geneview | rs778947880 |
scholar | rs778947880 |
rs778947880 | |
pharmgkb | rs778947880 |
gwascentral | rs778947880 |
openSNP | rs778947880 |
23andMe | rs778947880 |
SNPshot | rs778947880 |
SNPdbe | rs778947880 |
MSV3d | rs778947880 |
GWAS Ctlg | rs778947880 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs778947880(G;G) rs778947880(T;T) |
Alt | rs778947880(G;G) rs778947880(T;T) |
Reference | Rs778947880(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | MIB1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.19345768C>T |
CLNSRC | |
CLNACC | RCV000481876.1, |