Have questions? Visit https://www.reddit.com/r/SNPedia

rs7958311

From SNPedia

Orientationplus
Stabilizedplus
Make rs7958311(A;A)
Make rs7958311(A;G)
Make rs7958311(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position121167552
GeneP2RX7
is asnp
is mentioned by
dbSNPrs7958311
ebirs7958311
HLIrs7958311
Exacrs7958311
Varsomers7958311
Maprs7958311
PheGenIrs7958311
hapmaprs7958311
1000 genomesrs7958311
hgdprs7958311
ensemblrs7958311
gopubmedrs7958311
geneviewrs7958311
scholarrs7958311
googlers7958311
pharmgkbrs7958311
gwascentralrs7958311
openSNPrs7958311
23andMers7958311
23andMe allrs7958311
SNP Nexus

SNPshotrs7958311
SNPdbers7958311
MSV3drs7958311
GWAS Ctlgrs7958311
GMAF0.2893
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22447075OA-icon.png] Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity


[PMID 19319666OA-icon.png] Genetics of the P2X7 receptor and human disease.


[PMID 19838818OA-icon.png] Identification and characterization of a novel variant of the human P2X(7) receptor resulting in gain of function.


GET Evidence
P2RX7-R270H
aa_change Arg270His
aa_change_short R270H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.245213
summary



[PMID 27672203] P2X7R Gene Polymorphisms Are Associated with Increased Risk of Pulmonary Tuberculosis in the Tibetan Chinese Population.