rs6065906
|
|
6
|
|
|
20 |
45925376 |
downstream gene variant
|
T/A;C;G
|
snv |
|
|
0.800 |
1.000 |
6 |
2010 |
2019 |
rs737337
|
|
6
|
0.925 |
0.040 |
19 |
11236817 |
synonymous variant
|
T/C
|
snv |
0.15
|
0.20
|
0.800 |
1.000 |
6 |
2010 |
2019 |
rs103294
|
|
7
|
0.827 |
0.200 |
19 |
54293995 |
downstream gene variant
|
T/C
|
snv |
|
0.82
|
0.800 |
1.000 |
5 |
2012 |
2019 |
rs1042034
|
|
15
|
0.851 |
0.240 |
2 |
21002409 |
missense variant
|
C/T
|
snv |
0.70
|
0.78
|
0.800 |
1.000 |
5 |
2010 |
2019 |
rs12686004
|
|
6
|
1.000 |
0.040 |
9 |
104891145 |
intron variant
|
G/A
|
snv |
|
9.1E-02
|
0.800 |
1.000 |
5 |
2011 |
2019 |
rs13702
|
|
7
|
0.925 |
0.160 |
8 |
19966981 |
3 prime UTR variant
|
T/A;C
|
snv |
|
|
0.800 |
1.000 |
5 |
2011 |
2018 |
rs16942887
|
|
2
|
|
|
16 |
67894139 |
intron variant
|
G/A
|
snv |
|
0.15
|
0.800 |
1.000 |
5 |
2010 |
2019 |
rs17145738
|
|
11
|
0.851 |
0.200 |
7 |
73568544 |
3 prime UTR variant
|
C/T
|
snv |
|
0.11
|
0.800 |
1.000 |
5 |
2010 |
2019 |
rs17482753
|
|
8
|
1.000 |
0.080 |
8 |
19975135 |
regulatory region variant
|
G/T
|
snv |
|
8.8E-02
|
0.800 |
1.000 |
5 |
2008 |
2019 |
rs1800588
|
|
16
|
0.790 |
0.200 |
15 |
58431476 |
intron variant
|
C/G;T
|
snv |
0.30
|
|
0.800 |
1.000 |
5 |
2008 |
2019 |
rs1864163
|
|
10
|
0.882 |
0.120 |
16 |
56963321 |
intron variant
|
G/A
|
snv |
|
0.26
|
0.800 |
1.000 |
5 |
2008 |
2019 |
rs2144300
|
|
7
|
0.882 |
0.040 |
1 |
230159169 |
intron variant
|
C/T
|
snv |
|
0.44
|
0.800 |
1.000 |
5 |
2008 |
2018 |
rs247617
|
|
20
|
0.827 |
0.160 |
16 |
56956804 |
regulatory region variant
|
C/A
|
snv |
|
0.29
|
0.800 |
1.000 |
5 |
2013 |
2019 |
rs261334
|
|
5
|
|
|
15 |
58434545 |
intron variant
|
G/C
|
snv |
|
0.73
|
0.800 |
1.000 |
5 |
2010 |
2019 |
rs2678379
|
|
8
|
1.000 |
0.080 |
2 |
21003688 |
intron variant
|
A/G
|
snv |
|
0.76
|
0.800 |
1.000 |
5 |
2012 |
2019 |
rs328
|
|
19
|
0.732 |
0.440 |
8 |
19962213 |
stop gained
|
C/G
|
snv |
9.2E-02
|
9.0E-02
|
0.800 |
1.000 |
5 |
2008 |
2019 |
rs4660293
|
|
5
|
|
|
1 |
39562508 |
non coding transcript exon variant
|
A/C;G
|
snv |
|
|
0.800 |
1.000 |
5 |
2010 |
2018 |
rs4759375
|
|
3
|
|
|
12 |
123311691 |
intron variant
|
C/T
|
snv |
|
7.8E-02
|
0.800 |
1.000 |
5 |
2010 |
2019 |
rs4775041
|
|
8
|
1.000 |
0.040 |
15 |
58382496 |
intron variant
|
G/C
|
snv |
|
0.24
|
0.800 |
1.000 |
5 |
2008 |
2019 |
rs4939883
|
|
5
|
1.000 |
0.040 |
18 |
49640844 |
TF binding site variant
|
T/C;G
|
snv |
|
|
0.800 |
1.000 |
5 |
2009 |
2019 |
rs581080
|
|
3
|
|
|
9 |
15305380 |
intron variant
|
G/C
|
snv |
|
0.72
|
0.800 |
1.000 |
5 |
2010 |
2019 |
rs651821
|
|
17
|
0.851 |
0.360 |
11 |
116791863 |
5 prime UTR variant
|
C/T
|
snv |
0.88
|
0.89
|
0.800 |
1.000 |
5 |
2012 |
2019 |
rs7134594
|
|
4
|
1.000 |
0.200 |
12 |
109562388 |
intron variant
|
C/G;T
|
snv |
|
|
0.800 |
1.000 |
5 |
2010 |
2019 |
rs10096633
|
|
8
|
1.000 |
0.040 |
8 |
19973410 |
regulatory region variant
|
C/T
|
snv |
|
0.22
|
0.800 |
1.000 |
4 |
2011 |
2019 |
rs11613352
|
|
9
|
0.827 |
0.160 |
12 |
57398797 |
intron variant
|
C/T
|
snv |
|
0.19
|
0.800 |
1.000 |
4 |
2010 |
2018 |