rs11598177
|
|
1
|
1.000 |
0.040 |
10 |
101220399 |
regulatory region variant
|
T/C
|
snv |
|
0.47
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs12432469
|
|
1
|
1.000 |
0.040 |
14 |
26807946 |
intron variant
|
A/G
|
snv |
|
0.24
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs12432472
|
|
1
|
1.000 |
0.040 |
14 |
26807959 |
intron variant
|
A/C
|
snv |
|
0.25
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1322330
|
|
1
|
1.000 |
0.040 |
10 |
101231902 |
intron variant
|
A/G
|
snv |
|
0.22
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1322332
|
|
1
|
1.000 |
0.040 |
10 |
101222891 |
downstream gene variant
|
T/C
|
snv |
|
0.50
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1400180
|
|
1
|
1.000 |
0.040 |
3 |
129285 |
intron variant
|
T/G
|
snv |
|
0.37
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1400182
|
|
1
|
1.000 |
0.040 |
3 |
128928 |
intron variant
|
C/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1407409
|
|
1
|
1.000 |
0.040 |
10 |
101225650 |
upstream gene variant
|
T/C
|
snv |
|
0.22
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1535462
|
|
1
|
1.000 |
0.040 |
10 |
101214115 |
TF binding site variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1568097
|
|
1
|
1.000 |
0.040 |
3 |
138468 |
intron variant
|
T/C
|
snv |
|
0.42
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1588962
|
|
1
|
1.000 |
0.040 |
3 |
142352 |
intron variant
|
T/C
|
snv |
|
0.32
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs17326792
|
|
1
|
1.000 |
0.040 |
3 |
131073 |
non coding transcript exon variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1878169
|
|
1
|
1.000 |
0.040 |
3 |
123429 |
intron variant
|
A/T
|
snv |
|
0.32
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs200590764
|
|
1
|
1.000 |
0.040 |
10 |
101216904 |
intergenic variant
|
-/T
|
delins |
|
6.6E-03
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs202193096
|
|
2
|
0.925 |
0.040 |
16 |
30089130 |
missense variant
|
G/A
|
snv |
2.2E-04
|
1.0E-04
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs2281894
|
|
1
|
1.000 |
0.040 |
1 |
109267922 |
synonymous variant
|
C/A
|
snv |
0.22
|
0.17
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs2393069
|
|
1
|
1.000 |
0.040 |
10 |
56359144 |
intron variant
|
C/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs3950032
|
|
1
|
1.000 |
0.040 |
10 |
101214352 |
TF binding site variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs4684051
|
|
1
|
1.000 |
0.040 |
3 |
136842 |
intron variant
|
A/G
|
snv |
|
0.34
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs594791
|
|
1
|
1.000 |
0.040 |
10 |
101236039 |
intron variant
|
T/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs751819844
|
|
1
|
1.000 |
0.040 |
7 |
81705724 |
missense variant
|
G/A
|
snv |
6.4E-05
|
2.8E-05
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs76319884
|
|
1
|
1.000 |
0.040 |
10 |
101216249 |
intergenic variant
|
C/G
|
snv |
|
8.8E-02
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs7639674
|
|
1
|
1.000 |
0.040 |
3 |
130837 |
non coding transcript exon variant
|
A/T
|
snv |
|
0.31
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs7914775
|
|
1
|
1.000 |
0.040 |
10 |
101216904 |
intergenic variant
|
C/T
|
snv |
|
8.8E-02
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs965084
|
|
1
|
1.000 |
0.040 |
3 |
125415 |
intron variant
|
G/C
|
snv |
|
0.31
|
0.700 |
1.000 |
1 |
2011 |
2011 |