rs1003421753
|
|
1
|
1.000 |
0.120 |
3 |
159989088 |
missense variant
|
C/T
|
snv |
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs1039312028
|
|
1
|
1.000 |
0.120 |
19 |
48955724 |
missense variant
|
G/A
|
snv |
|
1.4E-05
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1163350491
|
|
1
|
1.000 |
0.120 |
7 |
5880922 |
synonymous variant
|
C/T
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1185926926
|
|
1
|
1.000 |
0.120 |
21 |
45531748 |
missense variant
|
A/G
|
snv |
4.1E-06
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1250480918
|
|
1
|
1.000 |
0.120 |
21 |
45537803 |
synonymous variant
|
G/A
|
snv |
4.6E-06
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs13178127
|
|
1
|
1.000 |
0.120 |
5 |
83293613 |
intron variant
|
A/G
|
snv |
|
3.3E-02
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1320767909
|
|
1
|
1.000 |
0.120 |
21 |
45531982 |
missense variant
|
A/G
|
snv |
4.1E-06
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1335035506
|
|
1
|
1.000 |
0.120 |
17 |
18340207 |
missense variant
|
A/G
|
snv |
4.0E-06
|
1.4E-05
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1447708158
|
|
1
|
1.000 |
0.120 |
3 |
12604160 |
synonymous variant
|
C/T
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
2003 |
2003 |
rs146713238
|
|
1
|
1.000 |
0.120 |
5 |
132679861 |
missense variant
|
G/A
|
snv |
3.2E-05
|
8.4E-05
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs148701087
|
|
1
|
1.000 |
0.120 |
17 |
18340762 |
missense variant
|
G/A
|
snv |
6.4E-04
|
8.8E-04
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs150865017
|
|
1
|
1.000 |
0.120 |
3 |
126154627 |
missense variant
|
G/A;T
|
snv |
1.6E-05;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs16994592
|
|
1
|
1.000 |
0.120 |
19 |
6586487 |
intron variant
|
T/C
|
snv |
|
9.4E-02
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs17723799
|
|
1
|
1.000 |
0.120 |
5 |
149427514 |
non coding transcript exon variant
|
C/T
|
snv |
|
9.9E-02
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1785882
|
|
1
|
1.000 |
0.120 |
11 |
105052348 |
intron variant
|
A/T
|
snv |
|
0.45
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs1790192
|
|
1
|
1.000 |
0.120 |
11 |
118886482 |
non coding transcript exon variant
|
G/A;C
|
snv |
0.58
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1800893
|
|
1
|
1.000 |
0.120 |
1 |
206773822 |
intron variant
|
C/T
|
snv |
|
0.41
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1921310
|
|
1
|
1.000 |
0.120 |
2 |
161192690 |
intron variant
|
A/G
|
snv |
|
0.15
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs2237060
|
|
1
|
1.000 |
0.120 |
5 |
132635193 |
intron variant
|
T/G
|
snv |
|
0.29
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs2582869
|
|
1
|
1.000 |
0.120 |
13 |
108259797 |
intron variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs2637988
|
|
1
|
1.000 |
0.120 |
2 |
113119202 |
intron variant
|
G/A
|
snv |
|
0.53
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs2991216
|
|
1
|
1.000 |
0.120 |
9 |
90865745 |
intron variant
|
A/G
|
snv |
|
0.21
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs441399
|
|
1
|
1.000 |
0.120 |
15 |
90822992 |
regulatory region variant
|
G/A
|
snv |
|
0.50
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs4648022
|
|
1
|
1.000 |
0.120 |
4 |
102575280 |
intron variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs4934436
|
|
1
|
1.000 |
0.120 |
10 |
89023563 |
intergenic variant
|
C/T
|
snv |
|
0.60
|
0.010 |
1.000 |
1 |
2009 |
2009 |