rs10801153
|
|
3
|
0.925 |
0.080 |
1 |
192794818 |
intron variant
|
G/A
|
snv |
|
0.27
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs11059336
|
|
1
|
|
|
12 |
127745489 |
regulatory region variant
|
T/C
|
snv |
|
0.14
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs113209956
|
|
1
|
|
|
9 |
25211195 |
intergenic variant
|
C/T
|
snv |
|
5.4E-02
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1192553
|
|
1
|
|
|
1 |
17967858 |
intergenic variant
|
G/A
|
snv |
|
0.70
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1458103
|
|
1
|
|
|
11 |
81336231 |
intron variant
|
A/C
|
snv |
|
0.25
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs2463107
|
|
2
|
1.000 |
0.040 |
12 |
79699537 |
intron variant
|
A/C
|
snv |
|
0.36
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs2572431
|
|
2
|
1.000 |
0.040 |
8 |
11247568 |
downstream gene variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs34548976
|
|
2
|
1.000 |
0.040 |
7 |
31032854 |
intergenic variant
|
C/T
|
snv |
|
0.39
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs4813627
|
|
2
|
1.000 |
0.040 |
20 |
3074867 |
downstream gene variant
|
A/G
|
snv |
|
0.51
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs72711240
|
|
1
|
|
|
4 |
134774652 |
intron variant
|
C/T
|
snv |
|
2.2E-02
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs7766029
|
|
7
|
0.851 |
0.080 |
6 |
88137716 |
downstream gene variant
|
T/C
|
snv |
|
0.51
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs9875578
|
|
1
|
|
|
3 |
13752941 |
intergenic variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1202184
|
|
7
|
0.851 |
0.120 |
7 |
87584585 |
intron variant
|
C/T
|
snv |
|
0.39
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs1922242
|
|
8
|
0.827 |
0.120 |
7 |
87544351 |
intron variant
|
A/T
|
snv |
|
0.43
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs1401663578
|
|
4
|
0.882 |
0.120 |
17 |
63483037 |
missense variant
|
A/G
|
snv |
|
1.4E-05
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs2451828
|
|
1
|
|
|
5 |
7448683 |
intron variant
|
C/T
|
snv |
|
2.7E-02
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs4822492
|
|
4
|
1.000 |
0.040 |
22 |
24447626 |
intron variant
|
C/G
|
snv |
|
0.47
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs5751876
|
|
16
|
0.742 |
0.320 |
22 |
24441333 |
synonymous variant
|
T/C
|
snv |
0.54
|
0.52
|
0.050 |
1.000 |
5 |
2008 |
2016 |
rs2298383
|
|
11
|
0.827 |
0.200 |
22 |
24429543 |
non coding transcript exon variant
|
C/A;T
|
snv |
|
|
0.020 |
1.000 |
2 |
2008 |
2019 |
rs3761422
|
|
4
|
1.000 |
0.040 |
22 |
24430704 |
intron variant
|
T/C
|
snv |
|
0.62
|
0.010 |
< 0.001 |
1 |
2010 |
2010 |
rs3930965
|
|
2
|
1.000 |
0.040 |
10 |
4971951 |
intron variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs900418273
|
|
8
|
0.807 |
0.120 |
11 |
113393764 |
missense variant
|
A/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs63750264
|
|
17
|
0.716 |
0.360 |
21 |
25891784 |
missense variant
|
C/A;G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2004 |
2004 |
rs63750579
|
|
13
|
0.742 |
0.280 |
21 |
25891856 |
missense variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs2306073
|
|
4
|
0.882 |
0.080 |
12 |
27402904 |
intron variant
|
C/T
|
snv |
|
0.37
|
0.010 |
1.000 |
1 |
2012 |
2012 |