rs2069561
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs2069561(A;A) |
Make rs2069561(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 132963038 |
Gene | TG |
is a | snp |
is | mentioned by |
dbSNP | rs2069561 |
dbSNP (classic) | rs2069561 |
ClinGen | rs2069561 |
ebi | rs2069561 |
HLI | rs2069561 |
Exac | rs2069561 |
Gnomad | rs2069561 |
Varsome | rs2069561 |
LitVar | rs2069561 |
Map | rs2069561 |
PheGenI | rs2069561 |
Biobank | rs2069561 |
1000 genomes | rs2069561 |
hgdp | rs2069561 |
ensembl | rs2069561 |
geneview | rs2069561 |
scholar | rs2069561 |
rs2069561 | |
pharmgkb | rs2069561 |
gwascentral | rs2069561 |
openSNP | rs2069561 |
23andMe | rs2069561 |
SNPshot | rs2069561 |
SNPdbe | rs2069561 |
MSV3d | rs2069561 |
GWAS Ctlg | rs2069561 |
GMAF | 0.3678 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs2069561(A;A) |
Alt | rs2069561(A;A) |
Reference | Rs2069561(G;G) |
Significance | Probable-non-pathogenic |
Disease | not specified Thyroid dyshormonogenesis |
Variation | info |
Gene | TG |
CLNDBN | not specified Thyroid dyshormonogenesis |
Reversed | 0 |
HGVS | NC_000008.10:g.133975283G>A |
CLNSRC | |
CLNACC | RCV000242253.1, RCV000305066.1, |