rs383830
|
|
3
|
0.882 |
0.040 |
5 |
100613278 |
intergenic variant
|
A/T
|
snv |
|
0.76
|
0.020 |
1.000 |
2 |
2012 |
2015 |
rs2075674
|
|
2
|
1.000 |
0.040 |
7 |
100627408 |
synonymous variant
|
G/A
|
snv |
0.18
|
0.16
|
0.010 |
< 0.001 |
1 |
2014 |
2014 |
rs7385804
|
|
14
|
0.851 |
0.120 |
7 |
100638347 |
intron variant
|
C/A
|
snv |
|
0.65
|
0.010 |
< 0.001 |
1 |
2014 |
2014 |
rs7801190
|
|
2
|
1.000 |
0.040 |
7 |
100860471 |
non coding transcript exon variant
|
C/G
|
snv |
|
9.9E-02
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs763802417
|
|
5
|
0.882 |
0.040 |
X |
100862805 |
missense variant
|
G/A
|
snv |
5.9E-06
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs2227631
|
|
13
|
0.742 |
0.200 |
7 |
101126257 |
upstream gene variant
|
A/G
|
snv |
|
0.54
|
0.020 |
1.000 |
2 |
2006 |
2018 |
rs1799889
|
|
31
|
0.649 |
0.600 |
7 |
101126430 |
upstream gene variant
|
A/G
|
snv |
|
|
0.020 |
1.000 |
2 |
2006 |
2018 |
rs8025174
|
|
1
|
1.000 |
0.040 |
15 |
101279548 |
upstream gene variant
|
C/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |
rs2288349
|
|
5
|
0.882 |
0.120 |
19 |
10146569 |
intron variant
|
G/A
|
snv |
0.36
|
0.35
|
0.010 |
< 0.001 |
1 |
2015 |
2015 |
rs3736234
|
|
4
|
0.851 |
0.040 |
12 |
10160535 |
non coding transcript exon variant
|
G/A
|
snv |
|
0.40
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs11053646
|
|
18
|
0.724 |
0.280 |
12 |
10160849 |
missense variant
|
C/G
|
snv |
0.11
|
0.13
|
0.030 |
1.000 |
3 |
2003 |
2011 |
rs2228612
|
|
12
|
0.763 |
0.160 |
19 |
10162696 |
missense variant
|
T/A;C;G
|
snv |
0.14
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs16999593
|
|
14
|
0.742 |
0.240 |
19 |
10180505 |
missense variant
|
T/C
|
snv |
2.4E-02
|
9.6E-03
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs10420321
|
|
2
|
0.925 |
0.080 |
19 |
10189741 |
intron variant
|
A/G
|
snv |
|
0.11
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1416580204
|
|
49
|
0.608 |
0.720 |
14 |
102250837 |
missense variant
|
C/T
|
snv |
4.0E-06
|
7.0E-06
|
0.040 |
0.500 |
4 |
2007 |
2016 |
rs1420101
|
|
8
|
0.827 |
0.280 |
2 |
102341256 |
synonymous variant
|
C/T
|
snv |
0.33
|
0.35
|
0.010 |
< 0.001 |
1 |
2013 |
2013 |
rs13114738
|
|
16
|
0.851 |
0.120 |
4 |
102363708 |
intron variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs28362491
|
|
56
|
0.592 |
0.720 |
4 |
102500998 |
non coding transcript exon variant
|
ATTG/-
|
delins |
|
|
0.020 |
1.000 |
2 |
2013 |
2016 |
rs223469
|
|
1
|
1.000 |
0.040 |
4 |
102778621 |
intergenic variant
|
T/C
|
snv |
|
0.99
|
0.010 |
< 0.001 |
1 |
2009 |
2009 |
rs12147254
|
|
4
|
0.851 |
0.240 |
14 |
102799329 |
intron variant
|
G/A
|
snv |
|
0.23
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs1799750
|
|
48
|
0.592 |
0.760 |
11 |
102799765 |
intron variant
|
C/-
|
delins |
|
0.50
|
0.020 |
1.000 |
2 |
2016 |
2019 |
rs1004467
|
|
13
|
0.790 |
0.280 |
10 |
102834750 |
non coding transcript exon variant
|
A/G
|
snv |
0.15
|
0.14
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs4919687
|
|
14
|
0.742 |
0.160 |
10 |
102835491 |
non coding transcript exon variant
|
G/A
|
snv |
|
0.25
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs3824755
|
|
5
|
0.925 |
0.120 |
10 |
102836092 |
intron variant
|
G/A;C;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs679620
|
|
17
|
0.716 |
0.360 |
11 |
102842889 |
missense variant
|
T/C
|
snv |
0.58
|
0.57
|
0.010 |
1.000 |
1 |
2009 |
2009 |