TABLE 1

Risk allele frequencies

Marker SNPGene regionAlleles*Risk allele frequency
Reference groups
CaucasianAfrican AmericanHispanicAsian/Pacific IslanderAmerican IndianHapMap CEUHapMap YRIGWAS white cohorts
n   2,001 716 595 151 85    
rs1111875 HHEX C/T 60.3 76.7 65.3 37.8 47.6 55.8 85.8 59.8 
rs7923837 HHEX G/A 63.4 90.3 57.7 36.9 50.6 62.5 100 62.3 
rs11037909 EXT2 T/C 72.9 84.5 54.6 55.1 22.2 70 84.2 72.9 
rs3740878 EXT2 T/C 72.8 89.3 55.1 55.1 22.6 69.8 92.4 72.8 
rs1113132 EXT2 C/G 73.1 90.0 44.7 44.9 77.4 70 92.5 73.3 
rs13266634 SLC30A8 C/T 71.0 89.3 76.8 64.3 79.3 75.0 94.2 69.9 
rs7480010 LOC387761 G/A 28.5 83.1 25.1 24.8 22.6 24.6 100 30.1 
rs10811661 CDKN2A/B T/C 84.8 93.9 87.0 67.2 91.5 79.2 100 83 
rs1470579 IGF2BP2 C/A 32.6 73.1 30.7 31.9 24.1 29.2 86.7 30 
rs7754840 CDKAL1 C/G 32.7 56.8 32.5 39.8 30.5 30.8 66.7 31 
Marker SNPGene regionAlleles*Risk allele frequency
Reference groups
CaucasianAfrican AmericanHispanicAsian/Pacific IslanderAmerican IndianHapMap CEUHapMap YRIGWAS white cohorts
n   2,001 716 595 151 85    
rs1111875 HHEX C/T 60.3 76.7 65.3 37.8 47.6 55.8 85.8 59.8 
rs7923837 HHEX G/A 63.4 90.3 57.7 36.9 50.6 62.5 100 62.3 
rs11037909 EXT2 T/C 72.9 84.5 54.6 55.1 22.2 70 84.2 72.9 
rs3740878 EXT2 T/C 72.8 89.3 55.1 55.1 22.6 69.8 92.4 72.8 
rs1113132 EXT2 C/G 73.1 90.0 44.7 44.9 77.4 70 92.5 73.3 
rs13266634 SLC30A8 C/T 71.0 89.3 76.8 64.3 79.3 75.0 94.2 69.9 
rs7480010 LOC387761 G/A 28.5 83.1 25.1 24.8 22.6 24.6 100 30.1 
rs10811661 CDKN2A/B T/C 84.8 93.9 87.0 67.2 91.5 79.2 100 83 
rs1470579 IGF2BP2 C/A 32.6 73.1 30.7 31.9 24.1 29.2 86.7 30 
rs7754840 CDKAL1 C/G 32.7 56.8 32.5 39.8 30.5 30.8 66.7 31 

Data are percent.

*

Putative risk allele listed first.

French, 3.

Scandinavian, 7. CEU, European ancestry. YRI, African ancestry.

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