rs863223794
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs863223794(-;-) |
Make rs863223794(-;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 218346897 |
Gene | TGFB2, TGFB2-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs863223794 |
dbSNP (classic) | rs863223794 |
ClinGen | rs863223794 |
ebi | rs863223794 |
HLI | rs863223794 |
Exac | rs863223794 |
Gnomad | rs863223794 |
Varsome | rs863223794 |
LitVar | rs863223794 |
Map | rs863223794 |
PheGenI | rs863223794 |
Biobank | rs863223794 |
1000 genomes | rs863223794 |
hgdp | rs863223794 |
ensembl | rs863223794 |
geneview | rs863223794 |
scholar | rs863223794 |
rs863223794 | |
pharmgkb | rs863223794 |
gwascentral | rs863223794 |
openSNP | rs863223794 |
23andMe | rs863223794 |
SNPshot | rs863223794 |
SNPdbe | rs863223794 |
MSV3d | rs863223794 |
GWAS Ctlg | rs863223794 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs863223794(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TGFB2 TGFB2-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.218520239delG |
CLNSRC | |
CLNACC | RCV000200166.1, |