rs121913308
|
|
6
|
0.827 |
0.120 |
10 |
43114492 |
missense variant
|
A/C;G;T
|
snv |
|
|
0.700 |
|
0 |
|
|
rs142698837
|
|
5
|
0.851 |
0.080 |
8 |
132869781 |
missense variant
|
G/A
|
snv |
7.6E-04
|
7.0E-04
|
0.700 |
|
0 |
|
|
rs35187787
|
|
6
|
0.827 |
0.120 |
16 |
68822063 |
missense variant
|
G/A;T
|
snv |
3.3E-03;
2.4E-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 |
|
|
rs587779826
|
|
5
|
0.851 |
0.360 |
11 |
108267344 |
splice donor variant
|
T/C
|
snv |
4.0E-06
|
|
0.700 |
|
0 |
|
|
rs6759952
|
|
2
|
1.000 |
0.080 |
2 |
217406996 |
intron variant
|
T/A;C
|
snv |
|
|
0.800 |
1.000 |
1 |
2013 |
2013 |
rs7037324
|
|
3
|
0.882 |
0.080 |
9 |
97896036 |
regulatory region variant
|
A/G
|
snv |
|
0.71
|
0.710 |
1.000 |
1 |
2015 |
2015 |
rs10122541
|
|
1
|
1.000 |
0.080 |
9 |
97865986 |
intergenic variant
|
G/A
|
snv |
|
0.68
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs10983700
|
|
2
|
1.000 |
0.080 |
9 |
97775173 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2010 |
2010 |
rs10984103
|
|
2
|
0.925 |
0.080 |
9 |
97876993 |
TF binding site variant
|
A/C
|
snv |
|
0.68
|
0.700 |
1.000 |
1 |
2009 |
2009 |
rs11693806
|
|
2
|
0.925 |
0.120 |
2 |
217427435 |
non coding transcript exon variant
|
C/A;G
|
snv |
|
0.65
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs12129938
|
|
1
|
1.000 |
0.080 |
1 |
233276815 |
intron variant
|
A/G
|
snv |
|
0.20
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs12348691
|
|
2
|
0.925 |
0.120 |
9 |
97846400 |
intron variant
|
G/A
|
snv |
|
0.63
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1443435
|
|
1
|
1.000 |
0.080 |
9 |
97855301 |
3 prime UTR variant
|
T/C
|
snv |
|
0.63
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1443438
|
|
8
|
0.827 |
0.080 |
9 |
97787746 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs2289261
|
|
1
|
1.000 |
0.080 |
15 |
67165147 |
intron variant
|
G/C;T
|
snv |
|
0.61
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs2466076
|
|
1
|
1.000 |
0.080 |
8 |
32575278 |
intron variant
|
G/T
|
snv |
|
0.53
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs368187
|
|
2
|
0.925 |
0.080 |
14 |
36063370 |
non coding transcript exon variant
|
G/A;C;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs56062135
|
|
8
|
0.790 |
0.200 |
15 |
67163292 |
intron variant
|
C/T
|
snv |
|
0.18
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs6793295
|
|
6
|
0.827 |
0.240 |
3 |
169800667 |
missense variant
|
T/C;G
|
snv |
0.37;
1.8E-04
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs7024345
|
|
2
|
0.925 |
0.080 |
9 |
97832956 |
intron variant
|
A/G
|
snv |
|
0.82
|
0.700 |
1.000 |
1 |
2009 |
2009 |
rs7030280
|
|
2
|
1.000 |
0.080 |
9 |
97772985 |
intron variant
|
C/T
|
snv |
|
0.72
|
0.700 |
1.000 |
1 |
2010 |
2010 |
rs73227498
|
|
1
|
1.000 |
0.080 |
5 |
112150207 |
intron variant
|
A/T
|
snv |
|
0.11
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs7848973
|
|
2
|
0.925 |
0.080 |
9 |
97826557 |
intron variant
|
A/G
|
snv |
|
0.67
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs7866436
|
|
2
|
0.925 |
0.080 |
9 |
97887814 |
intergenic variant
|
G/A
|
snv |
|
0.70
|
0.700 |
1.000 |
1 |
2013 |
2013 |