RS2305795 P2RY11

Health Risk Chr 19:10115375 snv intron variant

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What This Variant Does

"Common variants in P2RY11 are associated with narcolepsy. Found that rs2305795 G allele appears to l...

Associated Conditions

Cataplexy and narcolepsy

Population Frequencies

gnomAD ALL

57%

1kG AFR

65.7%

1kG ALL

65.6%

1kG AMR

69.7%

1kG EAS

67.7%

1kG EUR

40.2%

1kG SAS

66.1%

Other Variants in P2RY11