rs1312391542
|
|
2
|
0.925 |
0.120 |
6 |
106104897 |
missense variant
|
G/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs7765004
|
|
2
|
0.925 |
0.120 |
6 |
113750518 |
regulatory region variant
|
A/C
|
snv |
|
0.32
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs1057519695
|
|
35
|
0.641 |
0.520 |
1 |
114713907 |
missense variant
|
TT/CA;CC
|
mnv |
|
|
0.010 |
1.000 |
1 |
1997 |
1997 |
rs121913255
|
|
26
|
0.667 |
0.400 |
1 |
114713907 |
missense variant
|
T/A;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1057519834
|
|
31
|
0.658 |
0.480 |
1 |
114713908 |
missense variant
|
TG/CT
|
mnv |
|
|
0.010 |
1.000 |
1 |
1997 |
1997 |
rs11554290
|
|
59
|
0.583 |
0.600 |
1 |
114713908 |
missense variant
|
T/A;C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
1997 |
1997 |
rs121913254
|
|
31
|
0.658 |
0.440 |
1 |
114713909 |
stop gained
|
G/A;C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs121913237
|
|
50
|
0.611 |
0.560 |
1 |
114716126 |
missense variant
|
C/A;G;T
|
snv |
8.0E-06
|
|
0.010 |
1.000 |
1 |
1997 |
1997 |
rs121913250
|
|
25
|
0.683 |
0.440 |
1 |
114716127 |
missense variant
|
C/A;G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
1997 |
1997 |
rs1880030
|
|
2
|
0.925 |
0.120 |
12 |
122046634 |
intron variant
|
G/A
|
snv |
|
0.39
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs7712513
|
|
2
|
0.925 |
0.120 |
5 |
122582513 |
intergenic variant
|
G/T
|
snv |
|
0.71
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs1239470707
|
|
2
|
0.925 |
0.120 |
3 |
12416785 |
missense variant
|
C/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2736098
|
|
48
|
0.600 |
0.600 |
5 |
1293971 |
synonymous variant
|
C/T
|
snv |
0.29
|
0.22
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs12917
|
|
45
|
0.605 |
0.480 |
10 |
129708019 |
missense variant
|
C/T
|
snv |
0.14
|
0.14
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs895819
|
|
46
|
0.623 |
0.560 |
19 |
13836478 |
non coding transcript exon variant
|
T/A;C;G
|
snv |
0.34
|
0.38
|
0.010 |
1.000 |
1 |
2020 |
2020 |
rs121913377
|
|
480
|
0.354 |
0.840 |
7 |
140753335 |
missense variant
|
CA/AT;TT
|
mnv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs113488022
|
|
490
|
0.351 |
0.840 |
7 |
140753336 |
missense variant
|
A/C;G;T
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1178732315
|
|
3
|
0.882 |
0.240 |
1 |
155236381 |
missense variant
|
A/G
|
snv |
|
1.4E-05
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs6449182
|
|
6
|
0.807 |
0.160 |
4 |
15778830 |
intron variant
|
C/G
|
snv |
|
0.22
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs2910164
|
|
193
|
0.447 |
0.880 |
5 |
160485411 |
mature miRNA variant
|
C/G
|
snv |
0.71;
4.1E-06
|
0.70
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1800890
|
|
29
|
0.658 |
0.400 |
1 |
206776020 |
intron variant
|
A/T
|
snv |
|
0.32
|
0.020 |
1.000 |
2 |
2010 |
2013 |
rs1390458638
|
|
2
|
0.925 |
0.120 |
2 |
219216441 |
missense variant
|
G/A
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs2234922
|
|
42
|
0.630 |
0.440 |
1 |
225838705 |
missense variant
|
A/G;T
|
snv |
0.19;
2.8E-05
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs1800797
|
|
43
|
0.605 |
0.800 |
7 |
22726602 |
non coding transcript exon variant
|
A/G
|
snv |
|
0.72
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs1800795
|
|
140
|
0.494 |
0.840 |
7 |
22727026 |
intron variant
|
C/G
|
snv |
|
0.71
|
0.010 |
1.000 |
1 |
2015 |
2015 |