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Table 2 Haplotype analysis in five probands with TTN:c.12478del (P1.1-P5.1) and one first-degree relative (P4.2)

From: TTN:c.12478del in proximal I-band of titin represents a common molecular cause of dilated cardiomyopathy in Slovenian patients

Marker ID

P1.1

P2.1

P3.1

P4.1

P4.2

P5.1

HAPLOTYPE

rs4894127

G G

G A

A A

G G

G A

G A

/

rs895838

G G

G G

G G

C G

G G

G G

G

rs4893895

T T

T A

T A

T T

T T

T T

T

rs1839152

A A

A G

A G

A A

A A

A G

A

rs2885627

A G

A A

A G

A A

A A

A G

A

rs12623637

A A

G A

A A

A A

A A

A A

A

rs1398967

A G

A G

A G

A G

A A

A A

A

rs10930768

C A

C A

C A

C A

A A

A A

A

rs13422461

C T

C T

C T

C T

T T

T T

T

rs2885984

G A

A A

A A

G A

A A

G A

A

rs62173650

G G

G G

T G

G G

G G

G G

G

21xTG

20|24

20|24

20|24

20|27

20|24

20|27

20

rs6433659

A G

A G

A A

A A

A G

A A

A

rs7423941

A A

A A

A A

A G

A A

A G

A

16xATT

13|16

13|16

13|16

13|14

13|13

13|11

13

22xAC

24|20

24|17

24|20

24|18

24|24

24|19

24

rs2043547

T G

G G

T G

G G

G G

T G

G

rs6726222

T C

T T

T C

T T

T T

T C

T

rs334096

G A

G A

G A

G A

A A

A A

A

rs334122

G A

G A

G A

G A

G G

G G

G

rs334024

G A

G A

G A

A A

A A

A A

A

rs334624

C C

T C

T C

C C

C C

C C

C

variant

T delT

T delT

T delT

T delT

T delT

T delT

T delT

rs4894050

A G

G G

A G

G G

G G

G G

G

rs6433735

C T

C C

C T

C C

C C

C C

C

rs2046775

A C

A A

A A

A C

C C

A A

/

  1. PX.1 (X = family numerical identifier), proband; PX.X, relative of a family X. SNP markers are reported as “allele1” “allele2” identified at the locus. Di- and tri-nucleotide repeat markers are reported as number of repeats per “allele1” “allele2” observed at the locus