rs112445441
|
|
32
|
0.658 |
0.400 |
12 |
25245347 |
missense variant
|
C/A;G;T
|
snv |
|
|
0.700 |
|
0 |
|
|
rs1203145163
|
|
1
|
1.000 |
0.080 |
21 |
42363329 |
missense variant
|
C/A
|
snv |
|
7.0E-06
|
0.700 |
|
0 |
|
|
rs1400295986
|
|
2
|
0.925 |
0.080 |
5 |
112838233 |
missense variant
|
T/C
|
snv |
|
|
0.700 |
|
0 |
|
|
rs1555515731
|
|
4
|
0.882 |
0.160 |
16 |
68812189 |
frameshift variant
|
T/-
|
delins |
|
|
0.700 |
|
0 |
|
|
rs180177133
|
|
9
|
0.807 |
0.240 |
16 |
23614089 |
frameshift variant
|
T/-
|
delins |
1.2E-05
|
1.4E-05
|
0.700 |
|
0 |
|
|
rs202208566
|
|
1
|
1.000 |
0.080 |
12 |
109903156 |
missense variant
|
T/C
|
snv |
6.5E-04
|
1.7E-04
|
0.700 |
|
0 |
|
|
rs367807476
|
|
1
|
1.000 |
0.080 |
19 |
1223035 |
missense variant
|
C/G;T
|
snv |
9.2E-06
|
1.4E-05
|
0.700 |
|
0 |
|
|
rs372481703
|
|
1
|
1.000 |
0.080 |
5 |
112839106 |
missense variant
|
G/A
|
snv |
1.6E-05
|
1.4E-05
|
0.700 |
|
0 |
|
|
rs555607708
|
|
33
|
0.667 |
0.360 |
22 |
28695869 |
frameshift variant
|
G/-
|
del |
2.0E-03
|
1.8E-03
|
0.700 |
|
0 |
|
|
rs587780537
|
|
5
|
0.925 |
0.080 |
16 |
68810224 |
missense variant
|
G/A
|
snv |
|
|
0.700 |
|
0 |
|
|
rs10029005
|
|
1
|
1.000 |
0.080 |
4 |
124530209 |
intron variant
|
G/A
|
snv |
|
0.40
|
0.700 |
1.000 |
1 |
2020 |
2020 |
rs10509671
|
|
1
|
1.000 |
0.080 |
10 |
94309297 |
intron variant
|
T/G
|
snv |
|
0.24
|
0.700 |
1.000 |
1 |
2020 |
2020 |
rs1057941
|
|
18
|
0.701 |
0.280 |
1 |
155216951 |
non coding transcript exon variant
|
G/A;T
|
snv |
0.46
|
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs1108143
|
|
1
|
1.000 |
0.080 |
2 |
234557214 |
regulatory region variant
|
A/G
|
snv |
|
8.1E-02
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs140081212
|
|
2
|
0.925 |
0.080 |
1 |
155215184 |
non coding transcript exon variant
|
G/A
|
snv |
|
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs2285947
|
|
7
|
0.807 |
0.120 |
7 |
21544470 |
intron variant
|
G/A
|
snv |
|
0.44
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs2294693
|
|
3
|
1.000 |
0.080 |
6 |
41037763 |
intron variant
|
T/C
|
snv |
|
0.26
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs2376549
|
|
2
|
0.925 |
0.120 |
20 |
31411284 |
intron variant
|
C/T
|
snv |
|
0.42
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs2494938
|
|
11
|
0.752 |
0.240 |
6 |
40568389 |
intron variant
|
G/A
|
snv |
|
0.51
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs28933379
|
|
2
|
1.000 |
0.080 |
5 |
112838953 |
missense variant
|
G/A
|
snv |
|
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs6490061
|
|
2
|
0.925 |
0.120 |
12 |
111335541 |
intron variant
|
T/C
|
snv |
|
0.30
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs6897169
|
|
1
|
1.000 |
0.080 |
5 |
40726036 |
intron variant
|
C/A;T
|
snv |
|
0.24
|
0.700 |
1.000 |
1 |
2020 |
2020 |
rs7624041
|
|
1
|
1.000 |
0.080 |
3 |
94389819 |
intergenic variant
|
G/A
|
snv |
|
0.89
|
0.700 |
1.000 |
1 |
2020 |
2020 |
rs7712641
|
|
1
|
1.000 |
0.080 |
5 |
89607147 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs7849280
|
|
1
|
1.000 |
0.080 |
9 |
133251249 |
non coding transcript exon variant
|
A/G
|
snv |
|
|
0.700 |
1.000 |
1 |
2018 |
2018 |