rs6672995
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6672995(A;A) |
Make rs6672995(A;G) |
Make rs6672995(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 247457731 |
is a | snp |
is | mentioned by |
dbSNP | rs6672995 |
dbSNP (classic) | rs6672995 |
ClinGen | rs6672995 |
ebi | rs6672995 |
HLI | rs6672995 |
Exac | rs6672995 |
Gnomad | rs6672995 |
Varsome | rs6672995 |
LitVar | rs6672995 |
Map | rs6672995 |
PheGenI | rs6672995 |
Biobank | rs6672995 |
1000 genomes | rs6672995 |
hgdp | rs6672995 |
ensembl | rs6672995 |
geneview | rs6672995 |
scholar | rs6672995 |
rs6672995 | |
pharmgkb | rs6672995 |
gwascentral | rs6672995 |
openSNP | rs6672995 |
23andMe | rs6672995 |
SNPshot | rs6672995 |
SNPdbe | rs6672995 |
MSV3d | rs6672995 |
GWAS Ctlg | rs6672995 |
GMAF | 0.1322 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19098911] Common variants in the NLRP3 region contribute to Crohn's disease susceptibility.
[PMID 27819323] Donor and recipient genetic variants in NLRP3 associate with early acute rejection following kidney transplantation.