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rs10167914

From SNPedia

Orientationplus
Stabilizedplus
Make rs10167914(A;A)
Make rs10167914(A;G)
Make rs10167914(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome2
Position112805784
is asnp
is mentioned by
dbSNPrs10167914
dbSNP (old)rs10167914
ClinGenrs10167914
ebirs10167914
HLIrs10167914
Exacrs10167914
Gnomadrs10167914
Varsomers10167914
Maprs10167914
PheGenIrs10167914
Biobankrs10167914
1000 genomesrs10167914
hgdprs10167914
ensemblrs10167914
gopubmedrs10167914
geneviewrs10167914
scholarrs10167914
googlers10167914
pharmgkbrs10167914
gwascentralrs10167914
openSNPrs10167914
23andMers10167914
23andMe allrs10167914
SNPshotrs10167914
SNPdbers10167914
MSV3drs10167914
GWAS Ctlgrs10167914
Max Magnitude
? (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.