Table 3 Gamete Competition results across TGFBM2 in French HHT.

From: Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

SNP

Chr

Chr position

Gene

HHT1 and HHT2 families

HHT1 families

HHT2 families

    

P -value

N

AF

N

AF

P -value

N

AF

N

AF

P -value

N

AF

N

AF

rs1874804

1

212,572,219

SMYD2

0.29

C

0.8

T

0.2

0.5

C

0.8

T

0.2

0.3

C

0.8

T

0.2

rs3002297

1

212,602,684

PTPN14

0.46

G

0.8

A

0.2

0.68

G

0.8

A

0.2

0.15

G

0.7

A

0.3

rs3002300

1

212,605,233

PTPN14

0.23

T

0.8

A

0.2

0.76

T

0.8

A

0.2

0.048

T

0.8

A

0.3

rs2936017

1

212,615,305

PTPN14

0.27

T

0.8

C

0.2

0.89

T

0.8

C

0.3

0.047

T

0.7

C

0.3

rs2936018

1

212,627,975

PTPN14

0.082

C

0.8

T

0.2

0.12

C

0.8

T

0.2

0.043

C

0.8

T

0.2

rs2070065

1

212,877,867

CENPF

0.97

C

0.9

G

0.1

0.8

C

0.9

G

0.1

0.42

C

0.9

G

0.1

rs7289

1

212,903,733

CENPF

0.93

G

0.5

C

0.5

0.47

G

0.5

C

0.5

0.49

G

0.6

C

0.4

rs10746458

1

214,034,701

USH2A

0.18

G

0.6

A

0.5

0.11

G

0.5

A

0.5

0.23

G

0.6

A

0.4

rs1538639

1

214,100,944

USH2A

0.81

G

0.9

A

0.1

0.69

G

0.9

A

0.1

0.59

G

0.9

A

0.1

rs2068721

1

214,319,365

USH2A

0.98

A

0.6

C

0.4

0.94

A

0.6

C

0.4

0.58

A

0.6

C

0.4

rs452747

1

214,412,771

USH2A

0.15

C

0.9

T

0.1

0.1

C

0.9

T

0.1

0.19

C

0.9

T

0.1

rs414373

1

214,416,358

USH2A

0.12

T

0.9

C

0.1

0.099

T

0.9

C

0.1

0.36

T

0.9

C

0.1

rs301746

1

214,423,261

USH2A

0.019

C

1

T

0.1

0.014

C

0.9

T

0.1

0.78

C

0.9

T

0.1

rs400358

1

214,434,804

USH2A

0.15

C

0.9

T

0.1

0.11

C

0.9

T

0.1

0.18

C

0.9

T

0.1

rs700024

1

214,509,837

USH2A

0.87

G

0.9

C

0.1

0.65

G

0.9

C

0.1

0.25

G

0.9

C

0.1

rs17650989

1

214,534,250

USH2A

0.94

G

0.9

A

0.1

0.47

G

0.9

A

0.1

0.38

G

0.9

A

0.1

rs17651066

1

214,536,744

USH2A

0.86

A

0.9

C

0.1

0.97

A

0.9

C

0.1

0.66

A

0.9

C

0.1

  1. Abbreviations: AF, allele frequency; HHT, hereditary haemorrhagic telangiectasia; N, nucleotide; SNP, single nucleotide polymorphism.