Summary statistics for platelet-reactivity genome wide association study (<5 × 10−8)
Phenotype . | Variant ID . | Chr . | Position . | Predicted consequence . | Ref. allele . | Alt. allele . | Alt. allele frequency . | n . | Effect size (SD/ALT allele) . | SE (SD/ALT alleles) . | P . | Nearest gene . |
---|---|---|---|---|---|---|---|---|---|---|---|---|
ADP | rs12566888 | 1 | 156 869 047 | Intronic variant | G | T | 0.09 | 1341 | −0.391 | 0.0706 | 3.184 × 10−8 | PEAR1 |
ADP | rs7624918 | 3 | 56 901 292 | Intronic variant | C | T | 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) | G | A | 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) | G | A | 0.20 | 550 | 0.515 | 0.0698 | 1.66 × 10−13 | F2RL3 |
PAR-1 | rs10886430 | 10 | 121 010 256 | Intronic variant | A | G | 0.13 | 546 | 1.09 | 0.0821 | 2.75 × 10−40 | GRK5 |
Phenotype . | Variant ID . | Chr . | Position . | Predicted consequence . | Ref. allele . | Alt. allele . | Alt. allele frequency . | n . | Effect size (SD/ALT allele) . | SE (SD/ALT alleles) . | P . | Nearest gene . |
---|---|---|---|---|---|---|---|---|---|---|---|---|
ADP | rs12566888 | 1 | 156 869 047 | Intronic variant | G | T | 0.09 | 1341 | −0.391 | 0.0706 | 3.184 × 10−8 | PEAR1 |
ADP | rs7624918 | 3 | 56 901 292 | Intronic variant | C | T | 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) | G | A | 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) | G | A | 0.20 | 550 | 0.515 | 0.0698 | 1.66 × 10−13 | F2RL3 |
PAR-1 | rs10886430 | 10 | 121 010 256 | Intronic variant | A | G | 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.