Table 1.

Summary statistics for platelet-reactivity genome wide association study (<5 × 10−8)

PhenotypeVariant IDChrPositionPredicted consequenceRef. alleleAlt. alleleAlt. allele frequencynEffect size
(SD/ALT allele)
SE
(SD/ALT alleles)
PNearest gene
ADP rs12566888 156 869 047 Intronic variant 0.09 1341 −0.391 0.0706 3.184 × 10−8 PEAR1 
ADP rs7624918 56 901 292 Intronic variant 0.34 1341 0.284 0.0434 5.75 × 10−11 ARHGEF3 
CRP-XL rs1613662 19 55 536 595 Nonsynonymous variant
c.655C>T
p.(Pro219Ser) 
0.83 1329 0.923 0.0432 5.01 × 10−101 GP6 
PAR-4 rs773902 19 17 000 632 Nonsynonymous variant
c.358G>A
p.(Ala120Thr) 
0.20 550 0.515 0.0698 1.66 × 10−13 F2RL3 
PAR-1 rs10886430 10 121 010 256 Intronic variant 0.13 546 1.09 0.0821 2.75 × 10−40 GRK5 
PhenotypeVariant IDChrPositionPredicted consequenceRef. alleleAlt. alleleAlt. allele frequencynEffect size
(SD/ALT allele)
SE
(SD/ALT alleles)
PNearest gene
ADP rs12566888 156 869 047 Intronic variant 0.09 1341 −0.391 0.0706 3.184 × 10−8 PEAR1 
ADP rs7624918 56 901 292 Intronic variant 0.34 1341 0.284 0.0434 5.75 × 10−11 ARHGEF3 
CRP-XL rs1613662 19 55 536 595 Nonsynonymous variant
c.655C>T
p.(Pro219Ser) 
0.83 1329 0.923 0.0432 5.01 × 10−101 GP6 
PAR-4 rs773902 19 17 000 632 Nonsynonymous variant
c.358G>A
p.(Ala120Thr) 
0.20 550 0.515 0.0698 1.66 × 10−13 F2RL3 
PAR-1 rs10886430 10 121 010 256 Intronic variant 0.13 546 1.09 0.0821 2.75 × 10−40 GRK5 

Coordinates are based on GRCh37. Predicted consequences are based on GP6 transcript NM_001083899.2 and PAR-4 transcript NM_003950.4

Alt., alternative; Chr, chromosome; Ref., reference.

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