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Table 3 Summary of selected FOXP2 and CNTNAP2 SNPs

From: Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

Gene

Marker, AB ID

Physical position (dbSNP130)

Genetic environment

SNP alleles (Major/Minor)

Minor allele frequency

Hardy–Weinberg test p value

FOXP2

rs2035980, hCV1189578

113495736

Promoter, CPG Island

T/C

0.3630

0.2215

rs923875, hCV1115584

113522272

Promoter, CPG Island

A/C

0.4348

0.4624

rs12533005, hCV220195

113843291

Transcription Start Site

G/C

0.4535

0.0963

rs10230558, hCV1604741

114032985

PolyQ Region

A/T

0.4880

0.6047

rs7782412, hCV1604757

114077651

Zinc Finger

T/C

0.4420

0.5996

rs936146, hCV7598355

114081641

Zinc Finger

G/C

0.4144

0.1657

CNTNAP2

rs851715, hCV2669966

147157839

Betw. Exons 13 and 14

A/G

0.3413

1.0000

rs2710102, hCV11430714

147205323

Betw. Exons 13 and 14

C/T

0.4827

0.9181

rs17236239, hCV34470590

147213238

Betw. Exons 13 and 14

A/G

0.3493

0.8202

rs4431523, hCV32080083

147228099

Betw. Exons 13 and 14

T/C

0.3293

0.8150