rs11249006
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11249006(A;A) |
Make rs11249006(A;G) |
Make rs11249006(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 24155984 |
Gene | IFNLR1, LOC107985738 |
is a | snp |
is | mentioned by |
dbSNP | rs11249006 |
dbSNP (classic) | rs11249006 |
ClinGen | rs11249006 |
ebi | rs11249006 |
HLI | rs11249006 |
Exac | rs11249006 |
Gnomad | rs11249006 |
Varsome | rs11249006 |
LitVar | rs11249006 |
Map | rs11249006 |
PheGenI | rs11249006 |
Biobank | rs11249006 |
1000 genomes | rs11249006 |
hgdp | rs11249006 |
ensembl | rs11249006 |
geneview | rs11249006 |
scholar | rs11249006 |
rs11249006 | |
pharmgkb | rs11249006 |
gwascentral | rs11249006 |
openSNP | rs11249006 |
23andMe | rs11249006 |
SNPshot | rs11249006 |
SNPdbe | rs11249006 |
MSV3d | rs11249006 |
GWAS Ctlg | rs11249006 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 26400298] Association of polymorphism within the interleukin-28 receptor alpha gene, but not in interleukin-28B, with lower urinary tract symptoms (LUTS) in Chinese