rs377767342
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs377767342(A;A) |
Make rs377767342(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 51065455 |
Gene | SMAD4 |
is a | snp |
is | mentioned by |
dbSNP | rs377767342 |
dbSNP (classic) | rs377767342 |
ClinGen | rs377767342 |
ebi | rs377767342 |
HLI | rs377767342 |
Exac | rs377767342 |
Gnomad | rs377767342 |
Varsome | rs377767342 |
LitVar | rs377767342 |
Map | rs377767342 |
PheGenI | rs377767342 |
Biobank | rs377767342 |
1000 genomes | rs377767342 |
hgdp | rs377767342 |
ensembl | rs377767342 |
geneview | rs377767342 |
scholar | rs377767342 |
rs377767342 | |
pharmgkb | rs377767342 |
gwascentral | rs377767342 |
openSNP | rs377767342 |
23andMe | rs377767342 |
SNPshot | rs377767342 |
SNPdbe | rs377767342 |
MSV3d | rs377767342 |
GWAS Ctlg | rs377767342 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs377767342(A;A) |
Alt | rs377767342(A;A) |
Reference | Rs377767342(G;G) |
Significance | Pathogenic |
Disease | JP and JP/HHT |
Variation | info |
Gene | SMAD4 |
CLNDBN | JP and JP/HHT |
Reversed | 0 |
HGVS | NC_000018.9:g.48591825G>A |
CLNSRC | ARUP SMAD4 |
CLNACC | RCV000021703.1, |
[PMID 15814640] SMAD4 as a prognostic marker in colorectal cancer.