rs10045431
|
|
3
|
0.851 |
0.240 |
5 |
159387525 |
intron variant
|
A/C
|
snv |
|
0.78
|
0.810 |
1.000 |
2 |
2008 |
2014 |
rs11167764
|
|
2
|
0.925 |
0.120 |
5 |
142099500 |
regulatory region variant
|
A/C
|
snv |
|
0.80
|
0.800 |
1.000 |
1 |
2010 |
2010 |
rs12948909
|
|
1
|
0.925 |
0.120 |
17 |
42418584 |
intron variant
|
A/C
|
snv |
|
0.24
|
0.700 |
1.000 |
1 |
2008 |
2008 |
rs16853571
|
|
1
|
1.000 |
0.040 |
4 |
41751113 |
intron variant
|
A/C
|
snv |
|
9.9E-02
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs16931910
|
|
1
|
1.000 |
0.040 |
9 |
114856029 |
intron variant
|
A/C
|
snv |
|
7.2E-02
|
0.700 |
1.000 |
1 |
2005 |
2005 |
rs17312836
|
|
1
|
1.000 |
0.040 |
16 |
50707551 |
intron variant
|
A/C
|
snv |
|
0.33
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs247660
|
|
1
|
1.000 |
0.040 |
5 |
85462322 |
upstream gene variant
|
A/C
|
snv |
|
0.21
|
0.700 |
1.000 |
1 |
2008 |
2008 |
rs3135499
|
|
1
|
0.882 |
0.160 |
16 |
50732216 |
splice donor variant
|
A/C
|
snv |
|
0.45
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs3763313
|
|
5
|
0.807 |
0.320 |
6 |
32408694 |
upstream gene variant
|
A/C
|
snv |
|
0.21
|
0.700 |
1.000 |
1 |
2008 |
2008 |
rs4807569
|
|
2
|
0.925 |
0.120 |
19 |
1123379 |
intron variant
|
A/C
|
snv |
|
0.25
|
0.710 |
1.000 |
1 |
2008 |
2010 |
rs4855873
|
|
1
|
1.000 |
0.040 |
3 |
49421681 |
non coding transcript exon variant
|
A/C
|
snv |
|
0.43
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs7186163
|
|
1
|
1.000 |
0.040 |
16 |
50652646 |
downstream gene variant
|
A/C
|
snv |
|
0.63
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs9891119
|
|
2
|
0.882 |
0.120 |
17 |
42355962 |
intron variant
|
A/C
|
snv |
|
0.36
|
0.810 |
1.000 |
1 |
2013 |
2013 |
rs10512734
|
|
1
|
1.000 |
0.040 |
5 |
40393503 |
intergenic variant
|
A/C;G
|
snv |
|
0.29
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs11871801
|
|
1
|
1.000 |
0.040 |
17 |
42418754 |
intron variant
|
A/C;G
|
snv |
|
|
0.800 |
1.000 |
1 |
2010 |
2010 |
rs12720356
|
|
2
|
0.752 |
0.360 |
19 |
10359299 |
missense variant
|
A/C;G
|
snv |
6.1E-02;
4.0E-06
|
|
0.800 |
1.000 |
1 |
2010 |
2016 |
rs2302759
|
|
1
|
1.000 |
0.040 |
16 |
50793690 |
intron variant
|
A/C;G
|
snv |
4.0E-06;
0.79
|
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs394522
|
|
1
|
1.000 |
0.040 |
6 |
166984583 |
intron variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs7076156
|
|
1
|
0.925 |
0.120 |
10 |
62655424 |
missense variant
|
A/C;G
|
snv |
0.80
|
|
0.810 |
1.000 |
1 |
2011 |
2012 |
rs740495
|
|
1
|
1.000 |
0.040 |
19 |
1124836 |
intron variant
|
A/C;G
|
snv |
|
|
0.800 |
1.000 |
1 |
2010 |
2010 |
rs11465802
|
|
1
|
1.000 |
0.040 |
1 |
67219915 |
intron variant
|
A/C;T
|
snv |
|
|
0.800 |
1.000 |
1 |
2007 |
2007 |
rs1373692
|
|
1
|
1.000 |
0.040 |
5 |
40431081 |
non coding transcript exon variant
|
A/C;T
|
snv |
|
|
0.800 |
1.000 |
1 |
2007 |
2007 |
rs9926095
|
|
1
|
1.000 |
0.040 |
16 |
50645404 |
3 prime UTR variant
|
A/C;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs2076756
|
|
2
|
0.882 |
0.040 |
16 |
50722970 |
intron variant
|
A/G
|
snv |
|
0.17
|
0.830 |
1.000 |
6 |
2007 |
2019 |
rs2241880
|
|
1
|
0.627 |
0.600 |
2 |
233274722 |
missense variant
|
A/G
|
snv |
0.45
|
0.44
|
0.900 |
0.961 |
4 |
2007 |
2020 |