rs10020432
|
|
2
|
0.925 |
0.080 |
4 |
73455883 |
3 prime UTR variant
|
A/G
|
snv |
|
0.54
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs10433937
|
|
4
|
0.882 |
0.080 |
4 |
87308948 |
intron variant
|
T/A;C;G
|
snv |
|
|
0.010 |
< 0.001 |
1 |
2019 |
2019 |
rs1140409
|
|
2
|
0.925 |
0.080 |
17 |
64500552 |
missense variant
|
A/C
|
snv |
5.4E-02
|
5.0E-02
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs12104272
|
|
2
|
0.925 |
0.080 |
19 |
49644795 |
intron variant
|
G/A
|
snv |
|
0.44
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs2298839
|
|
2
|
0.925 |
0.080 |
4 |
73445127 |
splice region variant
|
A/G;T
|
snv |
0.54
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs2679757
|
|
2
|
0.925 |
0.080 |
8 |
102858590 |
intron variant
|
A/G
|
snv |
|
0.37
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs4646038
|
|
2
|
0.925 |
0.080 |
1 |
15506705 |
intron variant
|
C/T
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs571462252
|
|
2
|
0.925 |
0.080 |
12 |
52904720 |
missense variant
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2005 |
2005 |
rs57749775
|
|
6
|
0.851 |
0.080 |
12 |
52904822 |
missense variant
|
A/G;T
|
snv |
1.7E-03;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2003 |
2003 |
rs675520
|
|
2
|
0.925 |
0.080 |
6 |
137672095 |
non coding transcript exon variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs6834059
|
|
2
|
0.925 |
0.080 |
4 |
73435958 |
intron variant
|
C/G
|
snv |
|
0.23
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs8021276
|
|
2
|
0.925 |
0.080 |
14 |
92110162 |
upstream gene variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs376373278
|
|
3
|
0.882 |
0.120 |
17 |
58279015 |
missense variant
|
G/A;C
|
snv |
4.2E-06
|
|
0.020 |
1.000 |
2 |
2011 |
2012 |
rs972427414
|
|
3
|
0.882 |
0.120 |
17 |
58279379 |
missense variant
|
A/G
|
snv |
|
|
0.020 |
1.000 |
2 |
2011 |
2012 |
rs10945859
|
|
3
|
0.882 |
0.120 |
6 |
162721570 |
intron variant
|
T/C
|
snv |
|
0.17
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs121918664
|
|
4
|
0.851 |
0.120 |
5 |
1254395 |
missense variant
|
C/T
|
snv |
5.2E-05
|
9.1E-05
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1431315635
|
|
3
|
0.882 |
0.120 |
6 |
26092928 |
missense variant
|
C/T
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs1485766
|
|
3
|
0.882 |
0.120 |
4 |
176689730 |
intron variant
|
T/A;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs16851720
|
|
5
|
0.827 |
0.120 |
3 |
141744456 |
intron variant
|
A/C
|
snv |
|
0.21
|
0.010 |
< 0.001 |
1 |
2017 |
2017 |
rs2289030
|
|
6
|
0.882 |
0.120 |
12 |
94834510 |
non coding transcript exon variant
|
G/C
|
snv |
9.7E-02
|
6.3E-02
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs3844942
|
|
3
|
0.882 |
0.120 |
4 |
189571800 |
intergenic variant
|
T/C
|
snv |
|
|
0.010 |
< 0.001 |
1 |
2017 |
2017 |
rs755284374
|
|
3
|
0.882 |
0.120 |
6 |
26093122 |
missense variant
|
C/A;T
|
snv |
4.0E-06;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs767864210
|
|
3
|
0.882 |
0.120 |
4 |
94657500 |
missense variant
|
G/A;T
|
snv |
8.0E-05
|
2.1E-05
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs843645
|
|
5
|
0.827 |
0.120 |
2 |
54247527 |
intron variant
|
T/A;G
|
snv |
|
0.19
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs897206619
|
|
3
|
0.882 |
0.120 |
6 |
26093128 |
missense variant
|
C/T
|
snv |
|
3.5E-05
|
0.010 |
1.000 |
1 |
2011 |
2011 |