rs16347
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16347(-;-) |
Make rs16347(-;TGAA) |
Make rs16347(TGAA;TGAA) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 112774142 |
Gene | IL1A |
is a | snp |
is | mentioned by |
dbSNP | rs16347 |
dbSNP (classic) | rs16347 |
ClinGen | rs16347 |
ebi | rs16347 |
HLI | rs16347 |
Exac | rs16347 |
Gnomad | rs16347 |
Varsome | rs16347 |
LitVar | rs16347 |
Map | rs16347 |
PheGenI | rs16347 |
Biobank | rs16347 |
1000 genomes | rs16347 |
hgdp | rs16347 |
ensembl | rs16347 |
geneview | rs16347 |
scholar | rs16347 |
rs16347 | |
pharmgkb | rs16347 |
gwascentral | rs16347 |
openSNP | rs16347 |
23andMe | rs16347 |
SNPshot | rs16347 |
SNPdbe | rs16347 |
MSV3d | rs16347 |
GWAS Ctlg | rs16347 |
Merged from | Rs3783553 |
GMAF | 0.4275 |
Max Magnitude | 0 |
[PMID 23927441] Genetic variants in IL1A and IL1B contribute to the susceptibility to 2009 pandemic H1N1 influenza A virus [PMID 12837270] Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1 gene cluster.