rs1126797
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1126797(C;T) |
Make rs1126797(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 1494031 |
Gene | TPO |
is a | snp |
is | mentioned by |
dbSNP | rs1126797 |
dbSNP (classic) | rs1126797 |
ClinGen | rs1126797 |
ebi | rs1126797 |
HLI | rs1126797 |
Exac | rs1126797 |
Gnomad | rs1126797 |
Varsome | rs1126797 |
LitVar | rs1126797 |
Map | rs1126797 |
PheGenI | rs1126797 |
Biobank | rs1126797 |
1000 genomes | rs1126797 |
hgdp | rs1126797 |
ensembl | rs1126797 |
geneview | rs1126797 |
scholar | rs1126797 |
rs1126797 | |
pharmgkb | rs1126797 |
gwascentral | rs1126797 |
openSNP | rs1126797 |
23andMe | rs1126797 |
SNPshot | rs1126797 |
SNPdbe | rs1126797 |
MSV3d | rs1126797 |
GWAS Ctlg | rs1126797 |
GMAF | 0.376 |
Max Magnitude | 0 |
[PMID 24420335] Genetic analysis of thyroid peroxidase (TPO) gene in patients whose hypothyroidism was found in adulthood in West Bengal, India
ClinVar | |
---|---|
Risk | rs1126797(A;A) rs1126797(G;G) rs1126797(T;T) |
Alt | rs1126797(A;A) rs1126797(G;G) rs1126797(T;T) |
Reference | Rs1126797(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified Congenital hypothyroidism |
Variation | info |
Gene | TPO |
CLNDBN | not specified Congenital hypothyroidism |
Reversed | 0 |
HGVS | NC_000002.11:g.1497803C>T |
CLNSRC | |
CLNACC | RCV000252817.1, RCV000358553.1, |