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Table 2 Overview of the studied SNPs

From: Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson’s disease – a multicenter study

SNP

rs-ID

Genome position

Alleles d > D

Gene location

SNP type

Taqman assay

NFE2L2

 

Chr:2(−)

    

2

rs7557529

177843343

G > A

5′-region

C__436313_10

P1

rs35652124

177838319

A > G

Promoter (−653)

Regulatory1

Sequencing2

P2

rs6706649

177838317

G > A

Promoter (−651)

Regulatory1

Sequencing2

P3

rs6721961

177838283

C > A

Promoter (−617)

Regulatory1

Sequencing2

3

rs2886161

177836085

A > G

Intron 1

C__351881_10

4

rs1806649

177826398

G > A

Intron 1

C_11634983_10

5

rs2001350

177808671

A > G

Intron 1

C_11634985_10

6

rs10183914

177805912

G > A

Intron 3

C__157561_10

  1. The SNPs analyzed in the study are numbered according to gene location in reference [23]; SNPs 2 – 6 are tag SNPs; SNPs P1–P3 are functional promoter SNPs. Genome positions were obtained from the CEU population of the HapMap Genome Browser (Phase 1 & 2 full dataset). Alleles are given according to the sense sequence of the gene.
  2. 1See reference [25].
  3. 2See reference [23].