rs766024374
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs766024374(A;A) |
Make rs766024374(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 218346914 |
Gene | TGFB2, TGFB2-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs766024374 |
dbSNP (classic) | rs766024374 |
ClinGen | rs766024374 |
ebi | rs766024374 |
HLI | rs766024374 |
Exac | rs766024374 |
Gnomad | rs766024374 |
Varsome | rs766024374 |
LitVar | rs766024374 |
Map | rs766024374 |
PheGenI | rs766024374 |
Biobank | rs766024374 |
1000 genomes | rs766024374 |
hgdp | rs766024374 |
ensembl | rs766024374 |
geneview | rs766024374 |
scholar | rs766024374 |
rs766024374 | |
pharmgkb | rs766024374 |
gwascentral | rs766024374 |
openSNP | rs766024374 |
23andMe | rs766024374 |
SNPshot | rs766024374 |
SNPdbe | rs766024374 |
MSV3d | rs766024374 |
GWAS Ctlg | rs766024374 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs766024374(A;A) rs766024374(T;T) |
Alt | rs766024374(A;A) rs766024374(T;T) |
Reference | Rs766024374(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | TGFB2 TGFB2-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.218520256C>A |
CLNSRC | |
CLNACC | RCV000428017.1, |