rs730881952
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AG;AG) | 0 | common in clinvar |
Make rs730881952(-;-) |
Make rs730881952(-;AG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 18 |
Position | 51067110 |
Gene | SMAD4 |
is a | snp |
is | mentioned by |
dbSNP | rs730881952 |
dbSNP (classic) | rs730881952 |
ClinGen | rs730881952 |
ebi | rs730881952 |
HLI | rs730881952 |
Exac | rs730881952 |
Gnomad | rs730881952 |
Varsome | rs730881952 |
LitVar | rs730881952 |
Map | rs730881952 |
PheGenI | rs730881952 |
Biobank | rs730881952 |
1000 genomes | rs730881952 |
hgdp | rs730881952 |
ensembl | rs730881952 |
geneview | rs730881952 |
scholar | rs730881952 |
rs730881952 | |
pharmgkb | rs730881952 |
gwascentral | rs730881952 |
openSNP | rs730881952 |
23andMe | rs730881952 |
SNPshot | rs730881952 |
SNPdbe | rs730881952 |
MSV3d | rs730881952 |
GWAS Ctlg | rs730881952 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881952(-;-) |
Alt | rs730881952(-;-) |
Reference | Rs730881952(AG;AG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SMAD4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000018.9:g.48593480_48593481delAG |
CLNSRC | |
CLNACC | RCV000160956.2, |