rs10109414
|
|
5
|
1.000 |
0.080 |
8 |
23893638 |
regulatory region variant
|
C/T
|
snv |
|
0.37
|
0.700 |
1.000 |
1 |
2010 |
2010 |
rs10137082
|
|
2
|
0.925 |
0.080 |
14 |
23370824 |
upstream gene variant
|
C/T
|
snv |
|
0.23
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs10178409
|
|
2
|
1.000 |
0.080 |
2 |
73628380 |
downstream gene variant
|
G/T
|
snv |
|
0.26
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs1020120
|
|
2
|
1.000 |
0.080 |
9 |
84611173 |
intron variant
|
C/T
|
snv |
|
0.60
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs1020608562
|
|
9
|
0.807 |
0.160 |
3 |
46373738 |
missense variant
|
T/C
|
snv |
4.0E-06
|
|
0.020 |
1.000 |
2 |
2011 |
2016 |
rs102274
|
|
3
|
1.000 |
0.080 |
11 |
61790354 |
non coding transcript exon variant
|
T/C
|
snv |
|
0.28
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs102275
|
|
18
|
0.827 |
0.320 |
11 |
61790331 |
non coding transcript exon variant
|
T/C
|
snv |
|
0.47
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs1024611
|
|
63
|
0.568 |
0.800 |
17 |
34252769 |
upstream gene variant
|
A/G
|
snv |
|
0.28
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1033182
|
|
3
|
0.882 |
0.160 |
6 |
151873899 |
intron variant
|
G/A
|
snv |
|
0.26
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs10404257
|
|
2
|
0.925 |
0.080 |
19 |
38645846 |
upstream gene variant
|
G/A
|
snv |
|
0.50
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1042636
|
|
23
|
0.672 |
0.360 |
3 |
122284922 |
missense variant
|
A/G
|
snv |
0.15
|
9.0E-02
|
0.020 |
1.000 |
2 |
2002 |
2009 |
rs1042713
|
|
63
|
0.576 |
0.800 |
5 |
148826877 |
missense variant
|
G/A
|
snv |
0.42
|
0.43
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1044261
|
|
3
|
1.000 |
0.080 |
10 |
1019770 |
stop gained
|
C/T
|
snv |
5.0E-02
|
6.0E-02
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1044498
|
|
15
|
0.752 |
0.360 |
6 |
131851228 |
missense variant
|
A/C;G
|
snv |
0.19
|
|
0.010 |
< 0.001 |
1 |
2008 |
2008 |
rs1045642
|
|
214
|
0.456 |
0.840 |
7 |
87509329 |
synonymous variant
|
A/G;T
|
snv |
0.50
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs1047891
|
|
34
|
0.827 |
0.200 |
2 |
210675783 |
missense variant
|
C/A
|
snv |
0.30
|
0.33
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs104894833
|
|
11
|
0.776 |
0.280 |
X |
101403984 |
missense variant
|
C/G
|
snv |
1.2E-04
|
1.9E-05
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1049255
|
|
9
|
0.776 |
0.320 |
16 |
88643329 |
3 prime UTR variant
|
C/T
|
snv |
0.49
|
0.48
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1061170
|
|
72
|
0.561 |
0.720 |
1 |
196690107 |
missense variant
|
C/T
|
snv |
0.68
|
0.64
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs1066621
|
|
2
|
1.000 |
0.080 |
3 |
191708066 |
regulatory region variant
|
C/T
|
snv |
|
0.39
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs10774021
|
|
4
|
1.000 |
0.080 |
12 |
240132 |
intron variant
|
C/T
|
snv |
|
0.57
|
0.700 |
1.000 |
1 |
2010 |
2010 |
rs1077989
|
|
3
|
1.000 |
0.080 |
14 |
67509105 |
intron variant
|
A/C
|
snv |
|
0.39
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs10783124
|
|
1
|
1.000 |
0.080 |
1 |
99937719 |
intergenic variant
|
A/G
|
snv |
|
2.9E-02
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs10794720
|
|
4
|
1.000 |
0.080 |
10 |
1110225 |
intron variant
|
T/C
|
snv |
|
0.89
|
0.700 |
1.000 |
1 |
2010 |
2010 |
rs10808565
|
|
2
|
0.925 |
0.080 |
8 |
127995166 |
non coding transcript exon variant
|
C/T
|
snv |
|
0.31
|
0.010 |
1.000 |
1 |
2007 |
2007 |