rs6503525
|
|
2
|
0.925 |
0.080 |
17 |
39938921 |
intron variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs6503526
|
|
2
|
0.925 |
0.080 |
17 |
39958345 |
intron variant
|
C/T
|
snv |
|
0.41
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs6716266
|
|
1
|
1.000 |
0.080 |
2 |
69018096 |
intron variant
|
T/G
|
snv |
|
0.23
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs7209742
|
|
1
|
1.000 |
0.080 |
17 |
39952455 |
upstream gene variant
|
A/G
|
snv |
|
0.69
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs7218742
|
|
1
|
1.000 |
0.080 |
17 |
39958108 |
intron variant
|
A/G
|
snv |
|
0.70
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs7219923
|
|
4
|
0.882 |
0.160 |
17 |
39918265 |
non coding transcript exon variant
|
C/T
|
snv |
|
0.52
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs8065126
|
|
2
|
1.000 |
0.080 |
17 |
39942782 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs8067378
|
|
12
|
0.752 |
0.240 |
17 |
39895095 |
regulatory region variant
|
A/G
|
snv |
|
0.50
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs8076131
|
|
11
|
0.790 |
0.200 |
17 |
39924659 |
intron variant
|
G/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs8076474
|
|
1
|
1.000 |
0.080 |
17 |
39954981 |
intron variant
|
G/C
|
snv |
|
0.69
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs8079416
|
|
2
|
0.925 |
0.080 |
17 |
39936460 |
intron variant
|
T/C
|
snv |
|
0.45
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs8179521
|
|
1
|
1.000 |
0.080 |
2 |
127393348 |
intron variant
|
A/C;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs907092
|
|
3
|
0.925 |
0.080 |
17 |
39766006 |
synonymous variant
|
G/A
|
snv |
0.41
|
0.36
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs9303277
|
|
9
|
0.790 |
0.240 |
17 |
39820216 |
intron variant
|
C/T
|
snv |
|
0.52
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs9303281
|
|
4
|
0.882 |
0.160 |
17 |
39917793 |
non coding transcript exon variant
|
G/A
|
snv |
|
0.50
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs7216389
|
|
14
|
0.732 |
0.440 |
17 |
39913696 |
intron variant
|
C/T
|
snv |
|
0.60
|
0.080 |
1.000 |
8 |
2008 |
2018 |
rs7793837
|
|
1
|
1.000 |
0.080 |
7 |
30687161 |
intron variant
|
A/C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs569108
|
|
8
|
0.790 |
0.200 |
11 |
60095631 |
missense variant
|
A/G
|
snv |
4.7E-02
|
7.3E-02
|
0.020 |
1.000 |
2 |
2009 |
2016 |
rs1220579705
|
|
1
|
1.000 |
0.080 |
5 |
132674079 |
missense variant
|
C/T
|
snv |
|
|
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 |
2009 |
2009 |
rs1800471
|
|
48
|
0.597 |
0.840 |
19 |
41352971 |
missense variant
|
C/G;T
|
snv |
5.6E-02
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs1805011
|
|
8
|
0.776 |
0.320 |
16 |
27362551 |
missense variant
|
A/C;G;T
|
snv |
0.13;
1.2E-04;
3.6E-05
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs2378383
|
|
1
|
1.000 |
0.080 |
9 |
79424447 |
intergenic variant
|
A/C;G;T
|
snv |
|
|
0.810 |
1.000 |
1 |
2009 |
2009 |
rs571448378
|
|
5
|
0.882 |
0.120 |
17 |
74872110 |
stop gained
|
G/A;C
|
snv |
4.1E-06;
4.1E-06
|
1.4E-05
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs748245223
|
|
2
|
0.925 |
0.080 |
16 |
27363275 |
synonymous variant
|
C/T
|
snv |
4.1E-06
|
|
0.010 |
1.000 |
1 |
2009 |
2009 |