rs4986790
|
|
223
|
0.438 |
0.800 |
9 |
117713024 |
missense variant
|
A/G;T
|
snv |
6.1E-02;
4.0E-06
|
|
0.090 |
0.778 |
9 |
2004 |
2019 |
rs1800972
|
|
16
|
0.708 |
0.440 |
8 |
6877901 |
5 prime UTR variant
|
C/G;T
|
snv |
0.79
|
|
0.030 |
0.667 |
3 |
2015 |
2019 |
rs1805192
|
|
121
|
0.510 |
0.840 |
3 |
12379739 |
missense variant
|
C/G
|
snv |
|
|
0.020 |
1.000 |
2 |
2013 |
2016 |
rs1027009063
|
|
2
|
0.925 |
0.040 |
2 |
8802974 |
stop gained
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs10484879
|
|
5
|
0.827 |
0.160 |
6 |
52187159 |
intron variant
|
G/A;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs10760187
|
|
2
|
0.925 |
0.040 |
9 |
121803541 |
intergenic variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2012 |
2012 |
rs1126580
|
|
3
|
0.882 |
0.120 |
2 |
218136243 |
3 prime UTR variant
|
G/A;T
|
snv |
|
|
0.010 |
< 0.001 |
1 |
2017 |
2017 |
rs13145041
|
|
2
|
0.925 |
0.040 |
4 |
189616909 |
intergenic variant
|
A/C;G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1458766475
|
|
41
|
0.637 |
0.680 |
1 |
169732649 |
missense variant
|
C/G;T
|
snv |
4.0E-06;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs1800470
|
|
107
|
0.515 |
0.840 |
19 |
41353016 |
missense variant
|
G/A;C
|
snv |
0.55;
2.4E-04
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1800471
|
|
48
|
0.597 |
0.840 |
19 |
41352971 |
missense variant
|
C/G;T
|
snv |
5.6E-02
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1801274
|
|
46
|
0.597 |
0.800 |
1 |
161509955 |
missense variant
|
A/C;G
|
snv |
4.0E-06;
0.48
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs187238
|
|
48
|
0.602 |
0.680 |
11 |
112164265 |
intron variant
|
C/A;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs200215055
|
|
11
|
0.742 |
0.400 |
1 |
161626196 |
missense variant
|
C/A;G;T
|
snv |
1.5E-03;
1.2E-05;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs20417
|
|
57
|
0.576 |
0.600 |
1 |
186681189 |
non coding transcript exon variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs2228570
|
|
99
|
0.521 |
0.760 |
12 |
47879112 |
start lost
|
A/C;G;T
|
snv |
0.63
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs2234663
|
|
14
|
0.716 |
0.480 |
2 |
113130529 |
intron variant
|
ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC/-;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC
|
delins |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2277438
|
|
5
|
0.827 |
0.160 |
13 |
42581032 |
intron variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs2521634
|
|
3
|
0.882 |
0.040 |
7 |
24338421 |
intron variant
|
G/A;C
|
snv |
|
|
0.800 |
1.000 |
1 |
2013 |
2013 |
rs35068180
|
|
5
|
0.851 |
0.040 |
11 |
102845217 |
upstream gene variant
|
A/-;AA
|
delins |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs3853839
|
|
10
|
0.752 |
0.480 |
X |
12889539 |
3 prime UTR variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs396991
|
|
14
|
0.742 |
0.480 |
1 |
161544752 |
missense variant
|
A/C;G;T
|
snv |
0.33;
4.1E-06
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs61752717
|
|
72
|
0.583 |
0.840 |
16 |
3243407 |
missense variant
|
T/A;C
|
snv |
2.8E-04
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs6815464
|
|
2
|
0.925 |
0.120 |
4 |
1316113 |
intron variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs7041
|
|
64
|
0.576 |
0.800 |
4 |
71752617 |
missense variant
|
A/C;T
|
snv |
0.52;
4.0E-06
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |