rs1143678
|
|
1
|
1.000 |
0.080 |
16 |
31331684 |
missense variant
|
C/T
|
snv |
0.15
|
0.17
|
0.730 |
1.000 |
6 |
2008 |
2017 |
rs1143683
|
|
1
|
1.000 |
0.080 |
16 |
31325567 |
missense variant
|
C/T
|
snv |
0.16
|
0.16
|
0.730 |
1.000 |
4 |
2009 |
2013 |
rs10239340
|
|
1
|
1.000 |
0.080 |
7 |
129028456 |
intron variant
|
T/A;G
|
snv |
|
|
0.700 |
1.000 |
3 |
2008 |
2014 |
rs12537284
|
|
1
|
1.000 |
0.080 |
7 |
129077852 |
intergenic variant
|
G/A
|
snv |
|
0.11
|
0.800 |
1.000 |
3 |
2008 |
2014 |
rs13205210
|
|
1
|
1.000 |
0.080 |
6 |
34864079 |
missense variant
|
T/C
|
snv |
0.11
|
0.13
|
0.720 |
1.000 |
3 |
2011 |
2019 |
rs1385374
|
|
1
|
1.000 |
0.080 |
12 |
128816149 |
intron variant
|
C/T
|
snv |
|
9.1E-02
|
0.810 |
1.000 |
3 |
2009 |
2016 |
rs148833270
|
|
1
|
1.000 |
0.080 |
3 |
48467524 |
missense variant
|
C/T
|
snv |
6.4E-05
|
2.1E-05
|
0.700 |
1.000 |
3 |
2007 |
2013 |
rs35000415
|
|
1
|
1.000 |
0.080 |
7 |
128945562 |
intron variant
|
C/T
|
snv |
|
9.0E-02
|
0.700 |
1.000 |
3 |
2015 |
2017 |
rs3757173
|
|
1
|
1.000 |
0.080 |
6 |
137869017 |
intron variant
|
A/G
|
snv |
|
0.20
|
0.720 |
1.000 |
3 |
2012 |
2016 |
rs387619
|
|
1
|
1.000 |
0.080 |
11 |
35076646 |
intergenic variant
|
T/A;C
|
snv |
|
|
0.710 |
1.000 |
3 |
2011 |
2016 |
rs72556555
|
|
1
|
1.000 |
0.080 |
3 |
48467375 |
missense variant
|
G/A;C
|
snv |
2.0E-05;
2.0E-04
|
|
0.700 |
1.000 |
3 |
2007 |
2013 |
rs7444
|
|
2
|
1.000 |
0.080 |
22 |
21622645 |
3 prime UTR variant
|
T/C
|
snv |
|
0.32
|
0.700 |
1.000 |
3 |
2015 |
2017 |
rs762011967
|
|
1
|
1.000 |
0.080 |
3 |
48467128 |
missense variant
|
C/T
|
snv |
4.4E-05
|
4.2E-05
|
0.700 |
1.000 |
3 |
2007 |
2013 |
rs7726414
|
|
1
|
1.000 |
0.080 |
5 |
134096143 |
intergenic variant
|
C/T
|
snv |
|
0.15
|
0.710 |
1.000 |
3 |
2015 |
2017 |
rs9462027
|
|
1
|
1.000 |
0.080 |
6 |
34829464 |
intron variant
|
G/A
|
snv |
|
0.37
|
0.700 |
1.000 |
3 |
2015 |
2017 |
rs9652601
|
|
1
|
1.000 |
0.080 |
16 |
11080508 |
intron variant
|
G/A
|
snv |
|
0.34
|
0.700 |
1.000 |
3 |
2015 |
2017 |
rs10048743
|
|
1
|
1.000 |
0.080 |
2 |
213025508 |
intron variant
|
G/T
|
snv |
|
0.78
|
0.700 |
1.000 |
2 |
2015 |
2016 |
rs1059312
|
|
1
|
1.000 |
0.080 |
12 |
128794319 |
synonymous variant
|
A/G
|
snv |
0.44
|
0.43
|
0.700 |
1.000 |
2 |
2015 |
2017 |
rs10912578
|
|
1
|
1.000 |
0.080 |
1 |
173282717 |
intergenic variant
|
A/G
|
snv |
|
0.63
|
0.700 |
1.000 |
2 |
2015 |
2016 |
rs11644034
|
|
1
|
1.000 |
0.080 |
16 |
85939006 |
intron variant
|
G/A
|
snv |
|
0.19
|
0.710 |
0.500 |
2 |
2014 |
2015 |
rs11755393
|
|
2
|
1.000 |
0.080 |
6 |
34856859 |
missense variant
|
A/G;T
|
snv |
0.36
|
|
0.710 |
1.000 |
2 |
2009 |
2011 |
rs13239597
|
|
3
|
0.882 |
0.080 |
7 |
129055929 |
non coding transcript exon variant
|
C/A
|
snv |
|
9.0E-02
|
0.710 |
1.000 |
2 |
2013 |
2020 |
rs13306575
|
|
1
|
1.000 |
0.080 |
1 |
183563302 |
missense variant
|
G/A;C;T
|
snv |
1.9E-02;
4.0E-06;
4.0E-06
|
|
0.710 |
1.000 |
2 |
2015 |
2016 |
rs13332649
|
|
1
|
1.000 |
0.080 |
16 |
85933077 |
intron variant
|
A/G
|
snv |
|
0.18
|
0.700 |
1.000 |
2 |
2015 |
2016 |
rs1370031102
|
|
1
|
1.000 |
0.080 |
4 |
87982700 |
missense variant
|
C/T
|
snv |
4.0E-06
|
7.0E-06
|
0.020 |
0.500 |
2 |
2002 |
2017 |