Table 1 Genetic variants at six loci significantly associated with lobar brain volumes

From: A genome-wide association study identifies genetic loci associated with specific lobar brain volumes

Lobe

Annotation (nearby)

Gene

Rs-ID

Chr

Position

A1

A2

European ancestry meta-analysis

Multi-ethnic meta-analysis

Replication sample (n = 8,789)

        

Frq

Effect

SE

p

Frq

Effect

SE

p

N

R2 (%)

Frq

Effect

SE

p

Parietal

UTR3

ZIC4

rs2279829

3

147106319

T

C

0.21

−0.92

0.16

5.3 × 10−9

0.21

−0.95

0.15

4.4 × 10−10

16,015

0.24

0.22

−0.63

0.18

6.0 × 10−4

Temporal

Intronic

MSRB3

rs146354218

12

65793942

A

G

0.37

0.69

0.11

1.2 × 10−9

0.37

0.69

0.11

6.4 × 10−10

15,789

0.24

0.37

0.54

0.14

6.4 × 10−5

Occipital

Intergenic

DAAM1 (dist = 24302)

rs147148763a

14

59631075

G

GTTGT

0.13

−0.83

0.14

6.6 × 10−9

0.13

−0.85

0.14

2.9 × 10−9

15,220

0.23

0.12

−0.80

0.12

3.1 × 10−11

Occipital

Intronic

FGFRL1

rs74921869

4

1013382

A

G

0.2

−0.84

0.14

5.9 × 10−9

0.2

−0.82

0.14

6.2 × 10−9

12,424

0.27

0.19

−0.22

0.10

3.0 × 10−2

Occipital

Intergenic

CENPW (dist = 175626)

rs1337736

6

126845380

A

G

0.23

−0.64

0.12

8.1 × 10−8

0.23

−0.64

0.12

4.0 × 10−8

16,016

0.19

0.23

−0.46

0.09

8.0 × 10−7

Occipital

Upstream

MIR92B/THBS3

rs12411216

1

155164480

A

C

0.46

−0.52

0.10

3.9 × 10−8

0.46

−0.49

0.09

1.4 × 10−7

16,016

0.17

0.45

−0.19

0.08

1.6 × 10−2

  1. The allele frequency (frq) and effect size are given for A1. Effect sizes are given in units of cm3 per effect allele. Results are provided for the discovery samples and the meta-analysis of all European ancestry and the multi-ethnic meta-analysis. The variance explained gives the percentage variance explained of a SNP16
  2. A1 effect allele, A2 reference allele, Chr chromosome, Frq effect allele frequency, N number of individuals with genetic variant, p p value, Rs-ID reference SNP cluster ID, SE standard error
  3. aIn the replication sample, another significant variant in high LD (R2 = 0.99) with this variant was used (rs76341705, p value = 4.8 × 10−9)
  4. Abbreviations: effect allele (A1), reference allele (A2), chromosome (Chr), effect allele frequency (Frq), number of individuals with genetic variant (N), p-value (P), reference SNP cluster ID (Rs-ID), standard error (SE)