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. Author manuscript; available in PMC: 2018 Apr 1.
Published in final edited form as: Clin Genet. 2016 Jul 28;91(4):545–556. doi: 10.1111/cge.12820

Table 1.

All possible reportable disease risk values*

Disease Genetic Variant RR Family History RR** BMI RR Smoking RR Diabetes RR Number of risk variables
AMD 2.4, 6.0 4.0 NA 1.4, 2.0 NA 5
CAD 1.3, 1.7 1.2, 1.4 NA 2.1*** 1.7 6
DM1 0.08, 0.3 2.3; 6.6 NA NA NA 4
DM2 1.2, 1.3 1.3, 1.9 2.3, 5.9 NA NA 6
HH 27.0**** NA NA NA NA 1
LUP 1.4, 2.0 4.1, 11.3 NA 1.5 NA 5
MEL 1.7, 3.0 2.2 NA NA NA 3
PRO 1.5 1.9 NA NA NA 2
Total 14 11 2 4 1 32

RR: Relative Risk

NA: not applicable risk factor

*

Values for Caucasian population represented

**
Positive family history defined as follows 5:
  • AMD: one or more first-degree relatives with age-related macular degeneration
  • CAD: one or both parents diagnosed with coronary artery disease
  • DM2: one or both parents with type 2 diabetes
  • LUP: one or two or more first-degree relatives with a history of any of 11 autoimmune diseases
  • MEL: one or more first-degree relatives with melanoma
  • PRO: biological father or any brothers diagnosed with prostate cancer
***

RR varies by gender and race

****

RR only provided to males. Male heterozygotes and homozygote wild type received an RR of 1.0; females got absolute risk: homozygotes received 16% lifetime risk, heterozygotes and wild type homozygotes received a lifetime risk of 1%.

AMD: Age Related Macular Degeneration

CAD: Coronary Artery Disease

DM1: Type 1 Diabetes

DM2: Type 2 Diabetes

HH: Hemochromatosis

LUP: Systemic Lupus Erythematosus

MEL: Melanoma

PRO: Prostate cancer