rs222747
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs222747(C;C) |
Make rs222747(C;G) |
Make rs222747(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 3589906 |
Gene | TRPV1 |
is a | snp |
is | mentioned by |
dbSNP | rs222747 |
dbSNP (classic) | rs222747 |
ClinGen | rs222747 |
ebi | rs222747 |
HLI | rs222747 |
Exac | rs222747 |
Gnomad | rs222747 |
Varsome | rs222747 |
LitVar | rs222747 |
Map | rs222747 |
PheGenI | rs222747 |
Biobank | rs222747 |
1000 genomes | rs222747 |
hgdp | rs222747 |
ensembl | rs222747 |
geneview | rs222747 |
scholar | rs222747 |
rs222747 | |
pharmgkb | rs222747 |
gwascentral | rs222747 |
openSNP | rs222747 |
23andMe | rs222747 |
SNPshot | rs222747 |
SNPdbe | rs222747 |
MSV3d | rs222747 |
GWAS Ctlg | rs222747 |
GMAF | 0.3007 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 20034385] Polymorphisms in gene encoding TRPV1-receptor involved in pain perception are unrelated to chronic pancreatitis
[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.
[PMID 28284340] TRPV1 polymorphisms and risk of interferon β-induced flu-like syndrome in patients with relapsing-remitting multiple sclerosis.