rs2268475
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2268475(C;C) |
Make rs2268475(C;T) |
Make rs2268475(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 81105966 |
Gene | LOC101928462, TSHR |
is a | snp |
is | mentioned by |
dbSNP | rs2268475 |
dbSNP (classic) | rs2268475 |
ClinGen | rs2268475 |
ebi | rs2268475 |
HLI | rs2268475 |
Exac | rs2268475 |
Gnomad | rs2268475 |
Varsome | rs2268475 |
LitVar | rs2268475 |
Map | rs2268475 |
PheGenI | rs2268475 |
Biobank | rs2268475 |
1000 genomes | rs2268475 |
hgdp | rs2268475 |
ensembl | rs2268475 |
geneview | rs2268475 |
scholar | rs2268475 |
rs2268475 | |
pharmgkb | rs2268475 |
gwascentral | rs2268475 |
openSNP | rs2268475 |
23andMe | rs2268475 |
SNPshot | rs2268475 |
SNPdbe | rs2268475 |
MSV3d | rs2268475 |
GWAS Ctlg | rs2268475 |
GMAF | 0.3889 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22673349] Association between thyroid stimulating hormone receptor gene intron polymorphisms and autoimmune thyroid disease in a Chinese Han population