rs1881457
|
|
9
|
0.790 |
0.280 |
5 |
132656717 |
intron variant
|
A/C
|
snv |
|
0.21
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs2243268
|
|
3
|
0.882 |
0.040 |
5 |
132678271 |
intron variant
|
A/C
|
snv |
|
0.23
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs2032582
|
|
97
|
0.538 |
0.800 |
7 |
87531302 |
missense variant
|
A/C;T
|
snv |
0.54;
3.8E-02
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs993269089
|
|
1
|
1.000 |
0.040 |
1 |
6385564 |
missense variant
|
A/C;T
|
snv |
4.0E-06
|
|
0.010 |
< 0.001 |
1 |
2014 |
2014 |
rs867186
|
|
15
|
0.752 |
0.120 |
20 |
35176751 |
missense variant
|
A/G
|
snv |
0.10
|
9.7E-02
|
0.020 |
1.000 |
2 |
2014 |
2016 |
rs1128503
|
|
64
|
0.564 |
0.760 |
7 |
87550285 |
synonymous variant
|
A/G
|
snv |
0.54
|
0.63
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs5743810
|
|
21
|
0.689 |
0.360 |
4 |
38828729 |
missense variant
|
A/G
|
snv |
0.73
|
0.72
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs762513613
|
|
11
|
0.752 |
0.280 |
1 |
161591315 |
missense variant
|
A/G
|
snv |
4.2E-06
|
7.4E-06
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs76723693
|
|
3
|
0.882 |
0.160 |
X |
154533025 |
missense variant
|
A/G
|
snv |
5.3E-04
|
1.5E-03
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs9624472
|
|
2
|
0.925 |
0.040 |
22 |
24438763 |
splice region variant
|
A/G
|
snv |
|
0.10
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs4986790
|
|
223
|
0.438 |
0.800 |
9 |
117713024 |
missense variant
|
A/G;T
|
snv |
6.1E-02;
4.0E-06
|
|
0.020 |
0.500 |
2 |
2006 |
2017 |
rs2069718
|
|
14
|
0.742 |
0.320 |
12 |
68156382 |
intron variant
|
A/G;T
|
snv |
|
0.50
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs8179190
|
|
1
|
1.000 |
0.040 |
5 |
132680584 |
intron variant
|
AAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAATG/-
|
delins |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1800630
|
|
17
|
0.701 |
0.480 |
6 |
31574699 |
upstream gene variant
|
C/A
|
snv |
|
0.14
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs5743618
|
|
25
|
0.677 |
0.360 |
4 |
38797027 |
missense variant
|
C/A
|
snv |
0.53
|
0.51
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs9282801
|
|
1
|
1.000 |
0.040 |
17 |
27769447 |
intron variant
|
C/A
|
snv |
|
0.32
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs2243282
|
|
1
|
1.000 |
0.040 |
5 |
132680862 |
intron variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs1800925
|
|
37
|
0.627 |
0.560 |
5 |
132657117 |
non coding transcript exon variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs1799724
|
|
47
|
0.600 |
0.680 |
6 |
31574705 |
upstream gene variant
|
C/T
|
snv |
|
8.5E-02
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs2069728
|
|
2
|
0.925 |
0.120 |
12 |
68154004 |
intron variant
|
C/T
|
snv |
|
0.13
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs2070874
|
|
27
|
0.672 |
0.560 |
5 |
132674018 |
5 prime UTR variant
|
C/T
|
snv |
0.28
|
0.28
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs4986791
|
|
182
|
0.456 |
0.840 |
9 |
117713324 |
missense variant
|
C/T
|
snv |
5.7E-02
|
4.9E-02
|
0.010 |
1.000 |
1 |
2006 |
2006 |
rs708567
|
|
6
|
0.807 |
0.200 |
3 |
9918386 |
missense variant
|
C/T
|
snv |
0.46
|
0.51
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs8177374
|
|
22
|
0.672 |
0.520 |
11 |
126292948 |
missense variant
|
C/T
|
snv |
0.12
|
0.11
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs3138557
|
|
4
|
0.851 |
0.080 |
12 |
68158711 |
intron variant
|
CGAG/-
|
delins |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |