rs401681
|
|
17
|
0.620 |
0.640 |
5 |
1321972 |
intron variant
|
C/T
|
snv |
|
0.48
|
0.860 |
1.000 |
1 |
2010 |
2015 |
rs45430
|
|
1
|
1.000 |
0.040 |
21 |
41374154 |
intron variant
|
C/T
|
snv |
|
0.48
|
0.820 |
1.000 |
2 |
2011 |
2019 |
rs3219090
|
|
1
|
1.000 |
0.040 |
1 |
226376990 |
intron variant
|
T/C
|
snv |
|
0.58
|
0.820 |
1.000 |
1 |
2011 |
2013 |
rs7023329
|
|
2
|
0.790 |
0.160 |
9 |
21816529 |
intron variant
|
A/G
|
snv |
|
0.50
|
0.810 |
1.000 |
4 |
2009 |
2017 |
rs1801516
|
|
3
|
0.627 |
0.400 |
11 |
108304735 |
missense variant
|
G/A
|
snv |
0.11
|
0.11
|
0.810 |
1.000 |
2 |
2011 |
2017 |
rs910873
|
|
2
|
0.882 |
0.160 |
20 |
34583968 |
intron variant
|
G/A;C
|
snv |
|
|
0.810 |
0.667 |
2 |
2008 |
2017 |
rs17119461
|
|
1
|
1.000 |
0.040 |
10 |
105756594 |
intergenic variant
|
T/C
|
snv |
|
7.7E-02
|
0.810 |
1.000 |
1 |
2012 |
2014 |
rs4698934
|
|
1
|
1.000 |
0.040 |
4 |
105218230 |
intron variant
|
T/C
|
snv |
|
0.12
|
0.810 |
1.000 |
1 |
2014 |
2014 |
rs113488022
|
|
22
|
0.351 |
0.840 |
7 |
140753336 |
missense variant
|
A/C;G;T
|
snv |
4.0E-06
|
|
0.800 |
0.979 |
30 |
2002 |
2020 |
rs121913227
|
|
1
|
0.653 |
0.320 |
7 |
140753336 |
missense variant
|
AC/CT;TT
|
mnv |
|
|
0.800 |
1.000 |
22 |
2002 |
2020 |
rs121913377
|
|
2
|
0.354 |
0.840 |
7 |
140753335 |
missense variant
|
CA/AT;TT
|
mnv |
|
|
0.800 |
0.981 |
19 |
2002 |
2020 |
rs11554290
|
|
25
|
0.583 |
0.600 |
1 |
114713908 |
missense variant
|
T/A;C;G
|
snv |
|
|
0.800 |
1.000 |
16 |
1989 |
2019 |
rs1057519695
|
|
1
|
0.641 |
0.520 |
1 |
114713907 |
missense variant
|
TT/CA;CC
|
mnv |
|
|
0.800 |
1.000 |
14 |
1989 |
2019 |
rs258322
|
|
3
|
0.925 |
0.120 |
16 |
89689495 |
intron variant
|
A/G;T
|
snv |
|
|
0.800 |
1.000 |
6 |
2009 |
2017 |
rs1393350
|
|
6
|
0.851 |
0.160 |
11 |
89277878 |
intron variant
|
G/A
|
snv |
|
0.17
|
0.800 |
1.000 |
4 |
2009 |
2017 |
rs121913351
|
|
9
|
0.776 |
0.240 |
7 |
140781611 |
missense variant
|
C/A;G;T
|
snv |
4.0E-06
|
|
0.800 |
1.000 |
2 |
2013 |
2014 |
rs13016963
|
|
3
|
0.851 |
0.080 |
2 |
201298088 |
intron variant
|
A/G
|
snv |
|
0.59
|
0.800 |
1.000 |
2 |
2011 |
2017 |
rs16953002
|
|
1
|
0.882 |
0.080 |
16 |
54080912 |
intron variant
|
G/A
|
snv |
|
0.19
|
0.800 |
1.000 |
2 |
2013 |
2017 |
rs1885120
|
|
2
|
1.000 |
0.040 |
20 |
34989186 |
intron variant
|
C/G
|
snv |
|
0.96
|
0.800 |
1.000 |
2 |
2008 |
2017 |
rs2284063
|
|
3
|
0.851 |
0.160 |
22 |
38148291 |
non coding transcript exon variant
|
A/G
|
snv |
|
0.40
|
0.800 |
1.000 |
2 |
2009 |
2017 |
rs4785763
|
|
3
|
0.925 |
0.120 |
16 |
90000528 |
non coding transcript exon variant
|
A/C;T
|
snv |
|
|
0.800 |
1.000 |
2 |
2009 |
2017 |
rs7412746
|
|
1
|
1.000 |
0.040 |
1 |
150887995 |
intron variant
|
C/T
|
snv |
|
0.41
|
0.800 |
1.000 |
2 |
2011 |
2017 |
rs1057519834
|
|
1
|
0.658 |
0.480 |
1 |
114713908 |
missense variant
|
TG/CT
|
mnv |
|
|
0.800 |
1.000 |
1 |
2005 |
2019 |
rs121913315
|
|
5
|
0.882 |
0.160 |
19 |
1220488 |
missense variant
|
G/A;T
|
snv |
|
|
0.800 |
1.000 |
1 |
1999 |
1999 |
rs13097028
|
|
1
|
1.000 |
0.040 |
3 |
169747154 |
regulatory region variant
|
C/T
|
snv |
|
0.38
|
0.800 |
1.000 |
1 |
2014 |
2014 |