Gene

Chr

Position

SNP

Location

Alleles

Mutation

Disease/Condition

Ethnic Group

Reference

(hg38)

(MAF)

PPARα

22

46218377

rs1800206

exon 5

C

c.484C >G

Hypertriglyceridemia,

Dyslipidemia,

Han Chinese

[10] [11] [16] [38] [39]

NM_005036.4

G (0.02)

p.Leu162Val

low-density

lipoprotein-cholesterol

PPARδ

6

35411001

rs2016520

5'UTR

A

c.-87A >G

Obesity risk, intracerebral

hemorrhages

Han Chinese,

[9] [14] [17]

NM_006238.4

G (0.23)

male Han

Chinese

35428018

rs9794

3’UTR

C

c.*1939C >G

Hypertriglyceridemia,

obesity

Han Chinese

[10] [11] [17]

G (0.27)

PPARγ

3

12311699

rs10865710

promoter

C

c.-757C >G

Obesity risk,

systemic sclerosis,

Han Chinese,

[9] [13] [16]

NM_138712.3

G (0.23)

low-density

lipoprotein-cholesterol

Caucasian

12357908

rs12629751

intron 1

C

c.-2-21796C >T

Osteoarthritis

Southeast

Chinese

[12]

T (0.21)

12421677

rs709158

intron 2

A

c.1186 + 4523A >G

low-density

lipoprotein-cholesterol

Han Chinese

[16]

G (0.25)

12379739

rs1805192

exon 2

C

c.34C >G

Hypertriglyceridemia,

Dyslipidemia,

Han Chinese

[10] [11] [16]

G (0.26)

p.Pro12Ala

low-density

lipoprotein-cholesterol

12434058

rs3856806

exon 7

C

c.1347C >T

Hypertriglyceridemia,

Dyslipidemia,

Han Chinese

[10] [11] [16]

T (0.23)

p.His449His

low-density

lipoprotein-cholesterol