rs765686939
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs765686939(C;C) |
Make rs765686939(C;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 139872234 |
Gene | TBXAS1 |
is a | snp |
is | mentioned by |
dbSNP | rs765686939 |
dbSNP (classic) | rs765686939 |
ClinGen | rs765686939 |
ebi | rs765686939 |
HLI | rs765686939 |
Exac | rs765686939 |
Gnomad | rs765686939 |
Varsome | rs765686939 |
LitVar | rs765686939 |
Map | rs765686939 |
PheGenI | rs765686939 |
Biobank | rs765686939 |
1000 genomes | rs765686939 |
hgdp | rs765686939 |
ensembl | rs765686939 |
geneview | rs765686939 |
scholar | rs765686939 |
rs765686939 | |
pharmgkb | rs765686939 |
gwascentral | rs765686939 |
openSNP | rs765686939 |
23andMe | rs765686939 |
SNPshot | rs765686939 |
SNPdbe | rs765686939 |
MSV3d | rs765686939 |
GWAS Ctlg | rs765686939 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs765686939(A;A) rs765686939(C;C) |
Alt | rs765686939(A;A) rs765686939(C;C) |
Reference | Rs765686939(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TBXAS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.139572033G>C |
CLNSRC | |
CLNACC | RCV000238661.1, |