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Table 1 P2X 7 genotype distribution for the study subjects (N=16)

From: The P2X7 loss-of-function Glu496Ala polymorphism affects ex vivo cytokine release and protects against the cytotoxic effects of high ATP-levels

Glu496Ala

NullAllele (151+1g>t) rs35933842

Val76Ala rs175 25809

Arg117Trp rs28360445

Gly150Arg rs283 60447

His155Tyr rs208294

Glu186Lys rs28360451

Leu191Pro rs28 360452

Null Allele (699C→T) n.a.

Arg270Cys rs16950860

Arg307Gln rs28360457

Ala348Thr rs1718119

Thr357Ser rs2230911

Gln460Arg rs2230912

Ile568Asn rs1653624

No. of subjects

HOMO

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

2

HOMO

HET

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

3

HOMO

WT

WT

WT

WT

HET

WT

WT

WT

WT

WT

WT

WT

WT

WT

2

HOMO

WT

WT

WT

HET

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

1

HOMO

WT

WT

WT

HET

WT

WT

WT

HET

WT

WT

WT

WT

WT

WT

1

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

WT

7

  1. HOMO: Homozygous for the variant allele.
  2. HET: Heterozygous.
  3. WT: Wild-type.