rs4808708
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs4808708(A;A) |
Make rs4808708(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 17890877 |
Gene | SLC5A5 |
is a | snp |
is | mentioned by |
dbSNP | rs4808708 |
dbSNP (classic) | rs4808708 |
ClinGen | rs4808708 |
ebi | rs4808708 |
HLI | rs4808708 |
Exac | rs4808708 |
Gnomad | rs4808708 |
Varsome | rs4808708 |
LitVar | rs4808708 |
Map | rs4808708 |
PheGenI | rs4808708 |
Biobank | rs4808708 |
1000 genomes | rs4808708 |
hgdp | rs4808708 |
ensembl | rs4808708 |
geneview | rs4808708 |
scholar | rs4808708 |
rs4808708 | |
pharmgkb | rs4808708 |
gwascentral | rs4808708 |
openSNP | rs4808708 |
23andMe | rs4808708 |
SNPshot | rs4808708 |
SNPdbe | rs4808708 |
MSV3d | rs4808708 |
GWAS Ctlg | rs4808708 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26160439] The potential role of the sodium symporter gene polymorphism in the development of differentiated thyroid cancer
ClinVar | |
---|---|
Risk | rs4808708(A;A) |
Alt | rs4808708(A;A) |
Reference | Rs4808708(G;G) |
Significance | Probable-non-pathogenic |
Disease | not specified Thyroid Hormonogenesis Defect |
Variation | info |
Gene | SLC5A5 |
CLNDBN | not specified Thyroid Hormonogenesis Defect |
Reversed | 0 |
HGVS | NC_000019.9:g.18001686G>A |
CLNSRC | |
CLNACC | RCV000248822.1, RCV000354638.1, |