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Table 1 Summary statistics of demographic data for the eMERGE participants with PGRNSeq data by self-reported sex and race

From: Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network

 

Female

Male

Combined

 

(N=546)

(N=348)

(N=894)

Self-Reported Race

American Indian orAlaska Native

2 %(9)

1 %(2)

1 %(11)

Asian

9 %(50)

5 %(19)

8 %(69)

Black or African American

5 %(29)

3 %(12)

5 %(41)

Native Hawaiian or otherPacific Islander

0 %(2)

0 %(0)

0 %(2)

Unknown

1 %(4)

5 %(16)

2 %(20)

White

83 %(452)

86 %(299)

84 %(751)

Ethnicity

No

95 %(520)

94 %(326)

95 %(846)

Yes

4 %(24)

2 %(6)

3 %(30)

Unknown

0 %(2)

5 %(16)

2 %(18)

Hx a of LQTS

0 %(0)

1 %(2)

0 %(2)

Hx of Hypertension

79 %(429)

80 %(279)

79 %(708)

Hx of Arrhythmia

48 %(264)

53 %(186)

50 %(450)

Hx of AF

7 %(38)

14 %(47)

10 %(85)

Hx of CHF

1 %(6)

3 %(12)

2 %(18)

Median LDL \(> 155\frac {mg}{dL}\)

9 %(50)

6 %(22)

8 %(72)

Median Triglyceride\(> 22\frac {mg}{dL}\)

6 %(33)

11 %(40)

8 %(73)

Median CK \( > 174\frac {IU}{L}\)

1 %(4)

7 %(23)

3 %(27)

Median TSH \(> 4\frac {\mu g}{dL}\)

6 %(34)

4 %(13)

5 %(47)

Median INR >1.5

7 %(36)

11 %(40)

9 %(76)

Total PGx Variants(total variants)

75.8±15.9

74.3±12.8

75.2±14.7

Coding PGx Variants(coding variants)

11.6±4.2

11.4±3.5

11.5±3.9

Group Health PGx Variants (gh variants)

40.0±9.6

38.5±8.7

39.4±9.3

  1. The continuous variables total variants, coding variants, and gh variants are presented in terms of mean and ± standard deviation
  2. aHx = History found in the EHR