rs6927172
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6927172(C;C) |
Make rs6927172(C;G) |
Make rs6927172(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 6 |
Position | 137681038 |
is a | snp |
is | mentioned by |
dbSNP | rs6927172 |
dbSNP (classic) | rs6927172 |
ClinGen | rs6927172 |
ebi | rs6927172 |
HLI | rs6927172 |
Exac | rs6927172 |
Gnomad | rs6927172 |
Varsome | rs6927172 |
LitVar | rs6927172 |
Map | rs6927172 |
PheGenI | rs6927172 |
Biobank | rs6927172 |
1000 genomes | rs6927172 |
hgdp | rs6927172 |
ensembl | rs6927172 |
geneview | rs6927172 |
scholar | rs6927172 |
rs6927172 | |
pharmgkb | rs6927172 |
gwascentral | rs6927172 |
openSNP | rs6927172 |
23andMe | rs6927172 |
SNPshot | rs6927172 |
SNPdbe | rs6927172 |
MSV3d | rs6927172 |
GWAS Ctlg | rs6927172 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 24776844] Associations between functional polymorphisms in the NFκB signaling pathway and response to anti-TNF treatment in Danish patients with inflammatory bowel disease
[PMID 27799070] Capture Hi-C identifies a novel causal gene, IL20RA, in the pan-autoimmune genetic susceptibility region 6q23.