rs1255998
|
|
6
|
0.827 |
0.200 |
14 |
64227153 |
3 prime UTR variant
|
G/C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs3761422
|
|
4
|
1.000 |
0.040 |
22 |
24430704 |
intron variant
|
T/C
|
snv |
|
0.62
|
0.010 |
< 0.001 |
1 |
2010 |
2010 |
rs3798577
|
|
16
|
0.742 |
0.320 |
6 |
152099995 |
3 prime UTR variant
|
T/C
|
snv |
|
0.45
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1415931588
|
|
2
|
1.000 |
0.080 |
1 |
237377426 |
missense variant
|
A/T
|
snv |
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs193922888
|
|
2
|
1.000 |
0.040 |
19 |
38584976 |
missense variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs73598374
|
|
8
|
0.790 |
0.280 |
20 |
44651586 |
missense variant
|
C/A;G;T
|
snv |
7.1E-06;
6.2E-02
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs2470893
|
|
8
|
0.882 |
0.160 |
15 |
74727108 |
upstream gene variant
|
C/T
|
snv |
|
0.20
|
0.030 |
1.000 |
3 |
2012 |
2016 |
rs2472297
|
|
9
|
0.882 |
0.160 |
15 |
74735539 |
intergenic variant
|
C/T
|
snv |
|
0.16
|
0.030 |
1.000 |
3 |
2012 |
2017 |
rs4410790
|
|
9
|
0.882 |
0.160 |
7 |
17244953 |
intron variant
|
T/C
|
snv |
|
0.54
|
0.030 |
1.000 |
3 |
2012 |
2017 |
rs6968865
|
|
1
|
|
|
7 |
17247645 |
5 prime UTR variant
|
A/T
|
snv |
|
0.54
|
0.020 |
1.000 |
2 |
2012 |
2016 |
rs11724635
|
|
3
|
0.925 |
0.080 |
4 |
15735478 |
intron variant
|
C/A;G
|
snv |
|
0.43
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs16851030
|
|
1
|
|
|
1 |
203166324 |
3 prime UTR variant
|
C/T
|
snv |
|
7.3E-02
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2896905
|
|
1
|
|
|
12 |
40099614 |
intron variant
|
G/A;C
|
snv |
|
0.36
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs5030732
|
|
10
|
0.790 |
0.160 |
4 |
41257616 |
missense variant
|
C/A
|
snv |
0.24
|
0.16
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs4998386
|
|
2
|
1.000 |
0.040 |
16 |
9976688 |
intron variant
|
C/T
|
snv |
|
0.11
|
0.020 |
0.500 |
2 |
2014 |
2018 |
rs68157013
|
|
1
|
|
|
12 |
11092126 |
missense variant
|
C/G
|
snv |
0.69
|
0.27
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs71443637
|
|
1
|
|
|
12 |
11091595 |
missense variant
|
T/C
|
snv |
0.57
|
0.28
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1401116572
|
|
2
|
1.000 |
0.080 |
1 |
237441382 |
missense variant
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1495741
|
|
9
|
0.827 |
0.240 |
8 |
18415371 |
regulatory region variant
|
G/A
|
snv |
|
0.71
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs33949390
|
|
9
|
0.776 |
0.160 |
12 |
40320043 |
missense variant
|
G/A;C;T
|
snv |
1.6E-04;
1.9E-03;
8.0E-06
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs142310826
|
|
3
|
1.000 |
0.040 |
4 |
178481702 |
intergenic variant
|
T/A
|
snv |
|
1.7E-02
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs2470890
|
|
12
|
0.742 |
0.320 |
15 |
74755085 |
synonymous variant
|
T/C
|
snv |
|
0.57
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs2472299
|
|
2
|
1.000 |
0.040 |
15 |
74741059 |
intergenic variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs104893877
|
|
59
|
0.614 |
0.360 |
4 |
89828149 |
missense variant
|
C/T
|
snv |
|
|
0.010 |
< 0.001 |
1 |
2018 |
2018 |
rs10772420
|
|
1
|
|
|
12 |
11021677 |
missense variant
|
G/A
|
snv |
0.45
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |