{{Rsnum
|rsid=2305795
|Gene=EIF3G
|Chromosome=19
|position=10115376
|Orientation=plus
|GMAF=0.3623
|Gene_s=EIF3G,PPAN-P2RY11,P2RY11
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 32.7 | 46.9 | 20.4
| HCB | 44.5 | 46.7 | 8.8
| JPT | 42.5 | 48.7 | 8.8
| YRI | 31.3 | 49.7 | 19.0
| ASW | 40.4 | 49.1 | 10.5
| CHB | 44.5 | 46.7 | 8.8
| CHD | 46.8 | 45.0 | 8.3
| GIH | 38.6 | 39.6 | 21.8
| LWK | 45.5 | 48.2 | 6.4
| MEX | 44.8 | 46.6 | 8.6
| MKK | 33.3 | 42.3 | 24.4
| TSI | 33.3 | 54.9 | 11.8
| HapMapRevision=28
}}Common variants in [[P2RY11]] are associated with [[narcolepsy]]. {{PMID|21170044|OA=1
}} Found that [[rs2305795]] G allele appears to lower the risk of [[narcolepsy]].

This SNP is also in the intronal area of the [[EIF3G]] gene.

{{PMID Auto
|PMID=22177342
|Title=TCRA, P2RY11, and CPT1B/CHKB associations in Chinese narcolepsy.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}