Table 1 Frequencies of OCTN2 genetic variations in promoter region.

From: Identification of OCTN2 variants and their association with phenotypes of Crohn’s disease in a Korean population

rs Number

Variant

Minor

allele

Frequency

rs

Number

Variant

Minor

allele

Frequency

rs2631372

g.-2087G > C

C

0.313

rs4646298

g.-446C > T

T

0.260

rs2631371

g.-1974G > A

A

0.313

rs2631369

g.-399G > C

C

0.313

rs2631370

g.-1889T > C

T

0.427

rs2631368

g.-368T > G

G

0.313

rs186829555

g.-1679C > G

G

0.021

–

g.-299G > C

C

0.021

rs34786243

g.-945T > G

G

0.255

rs4646300

g.-234C > G

G

0.032

  1. Data was obtained from DNA samples from 48 unrelated Korean individuals.
  2. The position of the variant is based upon the translational start site.
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