rs12327843
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs12327843(C;C) |
Make rs12327843(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 17894103 |
Gene | SLC5A5 |
is a | snp |
is | mentioned by |
dbSNP | rs12327843 |
dbSNP (classic) | rs12327843 |
ClinGen | rs12327843 |
ebi | rs12327843 |
HLI | rs12327843 |
Exac | rs12327843 |
Gnomad | rs12327843 |
Varsome | rs12327843 |
LitVar | rs12327843 |
Map | rs12327843 |
PheGenI | rs12327843 |
Biobank | rs12327843 |
1000 genomes | rs12327843 |
hgdp | rs12327843 |
ensembl | rs12327843 |
geneview | rs12327843 |
scholar | rs12327843 |
rs12327843 | |
pharmgkb | rs12327843 |
gwascentral | rs12327843 |
openSNP | rs12327843 |
23andMe | rs12327843 |
SNPshot | rs12327843 |
SNPdbe | rs12327843 |
MSV3d | rs12327843 |
GWAS Ctlg | rs12327843 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26160439] The potential role of the sodium symporter gene polymorphism in the development of differentiated thyroid cancer
ClinVar | |
---|---|
Risk | rs12327843(C;C) |
Alt | rs12327843(C;C) |
Reference | Rs12327843(T;T) |
Significance | Probable-non-pathogenic |
Disease | Thyroid Hormonogenesis Defect |
Variation | info |
Gene | SLC5A5 |
CLNDBN | Thyroid Hormonogenesis Defect |
Reversed | 0 |
HGVS | NC_000019.9:g.18004912T>C |
CLNSRC | |
CLNACC | RCV000323427.1, |