rs10492367
|
|
3
|
0.882 |
0.040 |
12 |
27862037 |
regulatory region variant
|
G/T
|
snv |
|
0.12
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs10948172
|
|
3
|
0.882 |
0.040 |
6 |
44809954 |
intron variant
|
A/G
|
snv |
|
0.27
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs121912891
|
|
5
|
0.882 |
0.080 |
12 |
47976052 |
missense variant
|
C/T
|
snv |
|
7.0E-06
|
0.020 |
1.000 |
2 |
2008 |
2010 |
rs2820436
|
|
4
|
0.882 |
0.040 |
1 |
219467338 |
intergenic variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
2 |
2018 |
2018 |
rs10116772
|
|
4
|
0.882 |
0.080 |
9 |
4290541 |
intron variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs11718863
|
|
3
|
0.882 |
0.080 |
3 |
15175196 |
non coding transcript exon variant
|
A/G;T
|
snv |
0.21
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs12901071
|
|
3
|
0.882 |
0.160 |
15 |
67078051 |
intron variant
|
A/G
|
snv |
|
0.25
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs2622873
|
|
3
|
0.882 |
0.040 |
1 |
103000497 |
intron variant
|
T/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs2820443
|
|
8
|
0.882 |
0.120 |
1 |
219580167 |
regulatory region variant
|
T/C
|
snv |
|
0.23
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs3774354
|
|
3
|
0.882 |
0.080 |
3 |
52783659 |
intron variant
|
G/A
|
snv |
|
0.31
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs532464664
|
|
3
|
0.882 |
0.040 |
22 |
41238083 |
frameshift variant
|
-/GCCCGCGC
|
delins |
4.8E-03
|
1.2E-02
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs7533552
|
|
3
|
0.882 |
0.160 |
1 |
40307477 |
missense variant
|
T/A;C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs75621460
|
|
3
|
0.882 |
0.040 |
19 |
41327879 |
intron variant
|
G/A
|
snv |
|
2.0E-02
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs9930333
|
|
7
|
0.882 |
0.120 |
16 |
53766065 |
intron variant
|
T/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs9350591
|
|
2
|
0.925 |
0.040 |
6 |
75531811 |
intergenic variant
|
C/A;T
|
snv |
|
0.12
|
0.710 |
1.000 |
3 |
2015 |
2019 |
rs2521349
|
|
2
|
0.925 |
0.040 |
17 |
69507360 |
intron variant
|
G/A;T
|
snv |
|
|
0.700 |
1.000 |
2 |
2018 |
2018 |
rs2785988
|
|
2
|
0.925 |
0.040 |
1 |
219570796 |
intergenic variant
|
C/A
|
snv |
|
0.23
|
0.700 |
1.000 |
2 |
2018 |
2019 |
rs4907986
|
|
2
|
0.925 |
0.040 |
1 |
103084077 |
intron variant
|
C/T
|
snv |
|
0.49
|
0.020 |
1.000 |
2 |
2014 |
2017 |
rs10758594
|
|
2
|
0.925 |
0.040 |
9 |
4295583 |
intron variant
|
A/G
|
snv |
|
0.45
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs11105466
|
|
2
|
0.925 |
0.040 |
12 |
89933142 |
intron variant
|
G/A
|
snv |
|
0.37
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs11456119
|
|
2
|
0.925 |
0.040 |
7 |
96089185 |
intron variant
|
A/-;AA;AAA
|
delins |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs115740542
|
|
2
|
0.925 |
0.040 |
6 |
26123274 |
intron variant
|
T/C
|
snv |
|
3.6E-02
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs11732213
|
|
2
|
0.925 |
0.040 |
4 |
1702517 |
intron variant
|
T/C
|
snv |
|
0.16
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs11997261
|
|
2
|
0.925 |
0.040 |
8 |
8666851 |
intron variant
|
T/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs12193102
|
|
2
|
0.925 |
0.040 |
6 |
45177665 |
intron variant
|
C/G
|
snv |
|
0.33
|
0.700 |
1.000 |
1 |
2019 |
2019 |