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Table 6 The potential disease causing SNPs in dominant inheritance pattern for pedigree 2

From: Exome sequencing study revealed novel susceptibility loci in subarachnoid hemorrhage (SAH)

Chr

Pos

Function

Gene

SIFT

Pp2

LRT

MT

M-CAP

CADD

REVEL

1

1.5E+ 08

exonic

HIST2H2AC

0.00

0.10

N

D

0.024

8.0

0.15

1

1.52E+ 08

exonic

RPTN

0.01

0.02

.

N

0.003

16.3

0.01

1

1.57E+ 08

exonic

IQGAP3

0.00

1.00

D

D

0.154

35.0

0.84

1

1.62E+ 08

exonic

DUSP12

0.10

1.00

D

D

0.009

23.4

0.16

6

56,471,328

intronic

DST

0.01

0.17

N

.

0.033

12.0

0.10

7

20,782,555

exonic

ABCB5

0.00

0.99

D

D

0.039

27.8

0.70

7

29,132,261

exonic

CPVL

0.04

0.99

N

D

0.142

26.6

0.47

7

94,057,039

exonic

COL1A2

0.10

0.98

D

N

0.082

26.2

0.44

7

1.01E+ 08

exonic

MUC17

0.02

0.61

.

N

0.003

5.6

0.04

7

1.51E+ 08

exonic

CHPF2

0.03

0.89

D

D

0.049

23.3

0.32

8

90,936,937

exonic

OSGIN2

0.38

0.03

D

D

0.01

11.3

0.07

17

3,030,476

exonic

OR1G1

0.05

0.01

.

N

0

13.6

0.03

17

4,619,845

exonic

ARRB2

0.04

0.90

D

D

0.034

32.0

0.15

17

6,683,525

exonic

FBXO39

0.14

0.09

D

D

0.024

19.8

0.17

17

7,733,695

exonic

DNAH2

0.01

0.89

N

N

0.004

23.8

0.11