Table 2 Results of the association analysis for common/rare variants in MTA cohort by (A) single- and (B) multiple-locus linear mixed models.

From: Mutations in sphingolipid metabolism genes are associated with ADHD

(A)

Chr

SNP

Position (hg19)

Gene

Marker information

Single-locus linear mixed model

Ref/Alt

MAF

CR

HGVS nomenclature

β (SEβ)

P value

PFDR

14

rs74073730

88,429,817

GALC

G/A

0.016

1

c.1072C > T/p.Leu358Leu

0.52 (0.09)

1.65 × 10−8

2.26 × 10−6

2

rs4668077

169,439,848

CERS6

G/A

0.251

1

c.407 + 22016A > G/intronic variant

0.11 (0.02)

6.47 × 10−6

4.43 × 10−2

11

rs35785620

6,415,704

SMPD1

G/A

0.004

1

c.1763C > A/p.Thr588Lys

0.58 (0.17)

6.6 × 10−4

3.01 × 10−2

1

rs143078230

28,285,155

SMPDL3B

T/C

0.002

1

c.556T > C/p.Tyr186His

0.91 (0.29)

1.95 × 10−3

5.0 × 10−2

1

rs139609178

150,939,279

CERS2

G/A

0.002

1

c.801C > A/p.Val267Val

0.91 (0.29)

1.95 × 10−3

4.4 × 10−2

11

rs200333847

61,646,921

FADS3

C/T

0.002

1

c.385G > A/p.Asp129Asn

0.91 (0.29)

1.95 × 10−3

3.8 × 10−2

6

rs41273880

53,135,449

ELOVL5

T/C

0.002

1

c.779A > G/p.Tyr260Cys

0.91 (0.29)

1.95 × 10−3

3.3 × 10−2

(B)

Chr

SNP

Position (hg19)

Gene

Marker information

Multi-locus linear mixed model

Ref/Alt

MAF

CR

HGVS nomenclature

β (SEβ)

P value

PFDR

14

rs74073730

88,429,817

GALC

G/A

0.016

1

c.1072C > T/p.Leu358Leu

0.47 (0.09)

8.03 × 10−8

1.1 × 10−5

11

rs35785620

6,415,704

SMPD1

G/A

0.004

1

c.1763C > A/p.Thr588Lys

0.56 (0.15)

1.6 × 10−4

5.6 × 10−3

1

rs143078230

28,285,155

SMPDL3B

T/C

0.002

1

c.556T > C/p.Tyr186His

0.98 (0.25)

1.01 × 10−4

6.9 × 10−3

1

rs139609178

150,939,279

CERS2

G/A

0.002

1

c.801C > A/p.Val267Val

0.98 (0.25)

1.01 × 10−4

4.65 × 10−3

22

rs13057352

47,095,235

CERK

C/A

0.027

1

c.918G > T/p.Leu306Phe

0.21 (0.06)

1.51 × 10−3

3.45 × 10−2

  1. Chr chromosome, SNP single-nucleotide polymorphism, Ref/Alt reference/alternate allele, MAF minor allele frequency in this cohort, CR call rate, β regression coefficient, SEβ standard error of β, P P value, FDR false discovery rate, HGVS Human Genome Variation Society.