rs4915077
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 2 | Higher risk of hypothyroidism |
(T;T) |
Make rs4915077(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 107823394 |
Gene | VAV3 |
is a | snp |
is | mentioned by |
dbSNP | rs4915077 |
dbSNP (classic) | rs4915077 |
ClinGen | rs4915077 |
ebi | rs4915077 |
HLI | rs4915077 |
Exac | rs4915077 |
Gnomad | rs4915077 |
Varsome | rs4915077 |
LitVar | rs4915077 |
Map | rs4915077 |
PheGenI | rs4915077 |
Biobank | rs4915077 |
1000 genomes | rs4915077 |
hgdp | rs4915077 |
ensembl | rs4915077 |
geneview | rs4915077 |
scholar | rs4915077 |
rs4915077 | |
pharmgkb | rs4915077 |
gwascentral | rs4915077 |
openSNP | rs4915077 |
23andMe | rs4915077 |
SNPshot | rs4915077 |
SNPdbe | rs4915077 |
MSV3d | rs4915077 |
GWAS Ctlg | rs4915077 |
GMAF | 0.1423 |
Max Magnitude | 2 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22493691] Novel associations for hypothyroidism include known autoimmune risk Loci.