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Table 1 PLCXD3 SNPs identified by GWAS and reported by Bishop et al. (†) and those subsequently resequenced by Bishop et al. (‡) are shown. P values are given for the discovery and replication studies. SNP positions refer to GRCh37 build

From: Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study

SNP ID

Position

Genomic-control corrected P-value

Bishop et al. GWAS

85 vCJD cases vs. 1481 controls

Allelic Fisher Exact P-value

Bishop et al. Resequencing

120 vCJD cases vs. publicly available controls

Allelic Fisher Exact P-value

Bishop et al. Resequencing

109 sCJD cases vs. publicly available controls

Frequentist additive P- value

MRC Prion Unit GWAS

129 vCJD cases vs. 5020 UK controls

Frequentist additive P-value

MRC Prion Unit GWAS

2500 sCJD cases vs. 10548 controls

rs3863150

5:41506860

1.53 x 10−08

Not reported in study

Not reported in study

0.000949

0.282

rs688551

5:41506080

1.53 x 10−08

Not reported in study

Not reported in study

0.000949

0.282

rs10075789

5:41505703

1.53 x 10−08

Not reported in study

Not reported in study

0.00105

0.282

rs676328

5:41505689

1.53 x 10−08

Not reported in study

Not reported in study

0.00115

0.257

rs545358

5:41382691

Not reported in study

<2.2 x 10−16

2.01 x 10−5

0.668

0.788

rs319013

5:41382681

Not reported in study

1.25 x 10−06

4.69 x 10−8

0.331

0.139

rs76547469

5:41382647

Not reported in study

0.247

0.0702

0.545

0.624