rs10167914
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10167914(A;A) |
Make rs10167914(A;G) |
Make rs10167914(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 2 |
Position | 112805784 |
is a | snp |
is | mentioned by |
dbSNP | rs10167914 |
dbSNP (classic) | rs10167914 |
ClinGen | rs10167914 |
ebi | rs10167914 |
HLI | rs10167914 |
Exac | rs10167914 |
Gnomad | rs10167914 |
Varsome | rs10167914 |
LitVar | rs10167914 |
Map | rs10167914 |
PheGenI | rs10167914 |
Biobank | rs10167914 |
1000 genomes | rs10167914 |
hgdp | rs10167914 |
ensembl | rs10167914 |
geneview | rs10167914 |
scholar | rs10167914 |
rs10167914 | |
pharmgkb | rs10167914 |
gwascentral | rs10167914 |
openSNP | rs10167914 |
23andMe | rs10167914 |
SNPshot | rs10167914 |
SNPdbe | rs10167914 |
MSV3d | rs10167914 |
GWAS Ctlg | rs10167914 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29669463] Genetic Variation at Chromosome 2q13 and Its Potential Influence on Endometriosis Susceptibility Through Effects on the IL-1 Family.