rs74315401
|
|
32
|
0.683 |
0.320 |
20 |
4699525 |
missense variant
|
C/T
|
snv |
|
|
0.050 |
1.000 |
5 |
1995 |
2017 |
rs63751273
|
|
42
|
0.645 |
0.280 |
17 |
46010389 |
missense variant
|
C/T
|
snv |
|
|
0.040 |
1.000 |
4 |
1999 |
2017 |
rs104893877
|
|
59
|
0.614 |
0.360 |
4 |
89828149 |
missense variant
|
C/T
|
snv |
|
|
0.030 |
1.000 |
3 |
2017 |
2018 |
rs63750231
|
|
23
|
0.689 |
0.160 |
14 |
73198100 |
missense variant
|
A/C;G
|
snv |
|
|
0.030 |
1.000 |
3 |
2000 |
2016 |
rs63750376
|
|
7
|
0.827 |
0.120 |
17 |
45996657 |
missense variant
|
G/T
|
snv |
|
|
0.030 |
1.000 |
3 |
2003 |
2006 |
rs121918100
|
|
11
|
0.827 |
0.160 |
18 |
31595184 |
missense variant
|
T/C
|
snv |
|
|
0.020 |
1.000 |
2 |
2009 |
2015 |
rs1289324472
|
|
21
|
0.716 |
0.400 |
1 |
155236354 |
missense variant
|
T/C
|
snv |
|
1.4E-05
|
0.020 |
1.000 |
2 |
2014 |
2017 |
rs16944
|
|
92
|
0.531 |
0.920 |
2 |
112837290 |
upstream gene variant
|
A/G
|
snv |
|
0.57
|
0.020 |
1.000 |
2 |
2010 |
2011 |
rs1800587
|
|
43
|
0.620 |
0.720 |
2 |
112785383 |
upstream gene variant
|
G/A;C
|
snv |
|
0.32
|
0.020 |
1.000 |
2 |
2012 |
2013 |
rs1805192
|
|
121
|
0.510 |
0.840 |
3 |
12379739 |
missense variant
|
C/G
|
snv |
|
|
0.020 |
1.000 |
2 |
2010 |
2011 |
rs63750215
|
|
19
|
0.701 |
0.240 |
1 |
226885603 |
missense variant
|
A/T
|
snv |
|
|
0.020 |
1.000 |
2 |
2006 |
2008 |
rs63750635
|
|
5
|
0.851 |
0.120 |
17 |
46014286 |
missense variant
|
C/T
|
snv |
|
|
0.020 |
1.000 |
2 |
2002 |
2003 |
rs63751039
|
|
8
|
0.776 |
0.200 |
21 |
25891855 |
missense variant
|
T/C
|
snv |
|
|
0.020 |
1.000 |
2 |
2011 |
2012 |
rs1043202
|
|
3
|
0.882 |
0.080 |
12 |
54182178 |
missense variant
|
T/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs11136000
|
|
19
|
0.752 |
0.160 |
8 |
27607002 |
intron variant
|
T/C
|
snv |
|
0.56
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs112451138
|
|
2
|
0.925 |
0.080 |
14 |
73192667 |
missense variant
|
T/C
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs11931074
|
|
7
|
0.851 |
0.080 |
4 |
89718364 |
intron variant
|
G/A;C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs121909330
|
|
11
|
0.752 |
0.200 |
9 |
35065364 |
missense variant
|
G/A;C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs1233347077
|
|
4
|
0.851 |
0.160 |
19 |
44905894 |
missense variant
|
G/C
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
2006 |
2006 |
rs12976445
|
|
20
|
0.689 |
0.600 |
19 |
51693200 |
non coding transcript exon variant
|
T/C
|
snv |
|
0.45
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1401663578
|
|
4
|
0.882 |
0.120 |
17 |
63483037 |
missense variant
|
A/G
|
snv |
|
1.4E-05
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs17070145
|
|
10
|
0.790 |
0.120 |
5 |
168418786 |
intron variant
|
C/T
|
snv |
|
0.43
|
0.010 |
< 0.001 |
1 |
2009 |
2009 |
rs17518584
|
|
8
|
0.827 |
0.160 |
3 |
85555773 |
intron variant
|
C/T
|
snv |
|
0.50
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1799724
|
|
47
|
0.600 |
0.680 |
6 |
31574705 |
upstream gene variant
|
C/T
|
snv |
|
8.5E-02
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1799752
|
|
25
|
0.677 |
0.480 |
17 |
63488529 |
intron variant
|
-/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
|
delins |
|
|
0.010 |
1.000 |
1 |
2017 |
2017 |