rs10946737
|
|
1
|
|
|
6 |
24967012 |
intron variant
|
G/A
|
snv |
|
0.27
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs117806152
|
|
1
|
|
|
14 |
96214520 |
intron variant
|
A/C
|
snv |
|
1.2E-03
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1966862
|
|
8
|
0.790 |
0.120 |
4 |
85766908 |
intron variant
|
A/G
|
snv |
|
0.14
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs2741045
|
|
4
|
|
|
2 |
233671494 |
intron variant
|
C/T
|
snv |
|
0.22
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs4430924
|
|
1
|
|
|
2 |
61476721 |
intron variant
|
A/C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs7574865
|
|
59
|
0.574 |
0.720 |
2 |
191099907 |
intron variant
|
T/G
|
snv |
|
0.79
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs116561224
|
|
2
|
1.000 |
0.080 |
18 |
66962261 |
intergenic variant
|
A/G
|
snv |
|
7.4E-02
|
0.010 |
< 0.001 |
1 |
2017 |
2017 |
rs72631567
|
|
2
|
1.000 |
0.080 |
2 |
5092045 |
intergenic variant
|
A/G
|
snv |
|
4.5E-02
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1495741
|
|
9
|
0.827 |
0.240 |
8 |
18415371 |
regulatory region variant
|
G/A
|
snv |
|
0.71
|
0.030 |
1.000 |
3 |
2013 |
2017 |
rs2287622
|
|
16
|
0.724 |
0.240 |
2 |
168973818 |
missense variant
|
A/C;G;T
|
snv |
0.57
|
|
0.020 |
1.000 |
2 |
2013 |
2019 |
rs1050450
|
|
43
|
0.623 |
0.600 |
3 |
49357401 |
missense variant
|
G/A
|
snv |
0.28
|
0.30
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1214110864
|
|
2
|
1.000 |
0.040 |
7 |
87408071 |
missense variant
|
A/T
|
snv |
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs138642043
|
|
1
|
|
|
2 |
168964291 |
missense variant
|
C/T
|
snv |
3.4E-03
|
4.9E-03
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs2306283
|
|
16
|
0.742 |
0.320 |
12 |
21176804 |
missense variant
|
A/G;T
|
snv |
0.47
|
|
0.010 |
< 0.001 |
1 |
2019 |
2019 |
rs231775
|
|
115
|
0.504 |
0.720 |
2 |
203867991 |
missense variant
|
A/G;T
|
snv |
0.42;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2476601
|
|
121
|
0.498 |
0.800 |
1 |
113834946 |
missense variant
|
A/G
|
snv |
0.93
|
0.93
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs4148323
|
|
22
|
0.701 |
0.440 |
2 |
233760498 |
missense variant
|
G/A
|
snv |
2.2E-02
|
9.2E-03
|
0.010 |
< 0.001 |
1 |
2019 |
2019 |
rs4880
|
|
131
|
0.500 |
0.840 |
6 |
159692840 |
missense variant
|
A/G
|
snv |
0.48
|
0.47
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs9274407
|
|
3
|
0.925 |
0.120 |
6 |
32665055 |
missense variant
|
A/C;T
|
snv |
0.77
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs1800796
|
|
74
|
0.555 |
0.760 |
7 |
22726627 |
non coding transcript exon variant
|
G/C
|
snv |
|
9.9E-02
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs80292941
|
|
2
|
1.000 |
0.040 |
2 |
87480257 |
non coding transcript exon variant
|
A/T
|
snv |
|
0.16
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1041983
|
|
15
|
0.732 |
0.240 |
8 |
18400285 |
synonymous variant
|
C/T
|
snv |
0.34
|
0.36
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs17036170
|
|
2
|
1.000 |
0.080 |
3 |
12288912 |
5 prime UTR variant
|
G/A
|
snv |
|
1.1E-02
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs4553808
|
|
28
|
0.672 |
0.320 |
2 |
203866282 |
upstream gene variant
|
A/G;T
|
snv |
|
0.16
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs5742909
|
|
40
|
0.614 |
0.680 |
2 |
203867624 |
upstream gene variant
|
C/T
|
snv |
|
6.7E-02
|
0.010 |
1.000 |
1 |
2012 |
2012 |