rs4939827
|
|
25
|
0.708 |
0.160 |
18 |
48927093 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
8 |
2007 |
2019 |
rs3184504
|
|
92
|
0.572 |
0.600 |
12 |
111446804 |
missense variant
|
T/A;C;G
|
snv |
0.67
|
|
0.700 |
1.000 |
4 |
2015 |
2019 |
rs6066825
|
|
10
|
0.776 |
0.080 |
20 |
48723580 |
intron variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
4 |
2015 |
2019 |
rs1078643
|
|
10
|
0.776 |
0.080 |
17 |
10803924 |
missense variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
3 |
2019 |
2019 |
rs6469656
|
|
9
|
0.790 |
0.080 |
8 |
116635549 |
regulatory region variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
3 |
2014 |
2019 |
rs113488022
|
|
490
|
0.351 |
0.840 |
7 |
140753336 |
missense variant
|
A/C;G;T
|
snv |
4.0E-06
|
|
0.020 |
1.000 |
2 |
2013 |
2018 |
rs121913377
|
|
480
|
0.354 |
0.840 |
7 |
140753335 |
missense variant
|
CA/AT;TT
|
mnv |
|
|
0.020 |
1.000 |
2 |
2013 |
2018 |
rs12412391
|
|
9
|
0.790 |
0.080 |
10 |
99529178 |
intron variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
2 |
2014 |
2016 |
rs35107139
|
|
11
|
0.776 |
0.080 |
14 |
53952388 |
intron variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
2 |
2019 |
2019 |
rs45597035
|
|
10
|
0.776 |
0.080 |
13 |
73075014 |
intron variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
2 |
2019 |
2019 |
rs7226855
|
|
9
|
0.790 |
0.080 |
18 |
48927678 |
intron variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
2 |
2015 |
2019 |
rs10152518
|
|
9
|
0.790 |
0.080 |
15 |
67884824 |
intergenic variant
|
G/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1057941
|
|
18
|
0.701 |
0.280 |
1 |
155216951 |
non coding transcript exon variant
|
G/A;T
|
snv |
0.46
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs10951878
|
|
9
|
0.790 |
0.080 |
7 |
46887097 |
downstream gene variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs11150038
|
|
10
|
0.790 |
0.080 |
16 |
78042662 |
intron variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs11168936
|
|
17
|
0.708 |
0.280 |
12 |
49251457 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11196170
|
|
10
|
0.776 |
0.080 |
10 |
112962862 |
intron variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs115392158
|
|
17
|
0.708 |
0.280 |
6 |
31347004 |
intron variant
|
A/G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs115707823
|
|
19
|
0.701 |
0.320 |
6 |
30374976 |
intergenic variant
|
G/A
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs11610543
|
|
10
|
0.776 |
0.080 |
12 |
42740389 |
intergenic variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs11907546
|
|
17
|
0.708 |
0.280 |
20 |
34131991 |
upstream gene variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1222213359
|
|
62
|
0.574 |
0.720 |
6 |
43770966 |
missense variant
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2004 |
2004 |
rs12255141
|
|
9
|
0.790 |
0.080 |
10 |
112535133 |
intron variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1254244346
|
|
1
|
1.000 |
0.080 |
9 |
104822502 |
missense variant
|
G/A
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs12601991
|
|
17
|
0.708 |
0.280 |
17 |
37741642 |
intron variant
|
T/A;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |