rs876660150
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs876660150(-;TT) |
Make rs876660150(TT;TT) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 18 |
Position | 51078394 |
Gene | SMAD4 |
is a | snp |
is | mentioned by |
dbSNP | rs876660150 |
dbSNP (classic) | rs876660150 |
ClinGen | rs876660150 |
ebi | rs876660150 |
HLI | rs876660150 |
Exac | rs876660150 |
Gnomad | rs876660150 |
Varsome | rs876660150 |
LitVar | rs876660150 |
Map | rs876660150 |
PheGenI | rs876660150 |
Biobank | rs876660150 |
1000 genomes | rs876660150 |
hgdp | rs876660150 |
ensembl | rs876660150 |
geneview | rs876660150 |
scholar | rs876660150 |
rs876660150 | |
pharmgkb | rs876660150 |
gwascentral | rs876660150 |
openSNP | rs876660150 |
23andMe | rs876660150 |
SNPshot | rs876660150 |
SNPdbe | rs876660150 |
MSV3d | rs876660150 |
GWAS Ctlg | rs876660150 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876660150(TT;TT) |
Alt | rs876660150(TT;TT) |
Reference | Rs876660150(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | SMAD4 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000018.9:g.48604763_48604764dupTT |
CLNSRC | |
CLNACC | RCV000220401.1, |