rs1799983
|
|
246
|
0.430 |
0.880 |
7 |
150999023 |
missense variant
|
T/A;G
|
snv |
0.75
|
|
0.060 |
1.000 |
6 |
2010 |
2018 |
rs1320702652
|
|
11
|
0.752 |
0.160 |
15 |
43824536 |
missense variant
|
G/A
|
snv |
4.0E-06
|
|
0.040 |
1.000 |
4 |
2003 |
2014 |
rs1042714
|
|
54
|
0.597 |
0.640 |
5 |
148826910 |
stop gained
|
G/C;T
|
snv |
0.68
|
|
0.020 |
0.500 |
2 |
2010 |
2018 |
rs10927887
|
|
3
|
0.925 |
0.040 |
1 |
16024780 |
missense variant
|
A/C;G
|
snv |
0.55
|
|
0.020 |
1.000 |
2 |
2011 |
2013 |
rs10519210
|
|
1
|
1.000 |
0.040 |
15 |
63445726 |
intergenic variant
|
T/C;G
|
snv |
|
|
0.800 |
1.000 |
1 |
2010 |
2010 |
rs111033560
|
|
9
|
0.807 |
0.040 |
6 |
118559037 |
stop gained
|
T/G
|
snv |
1.6E-05
|
|
0.010 |
1.000 |
1 |
2003 |
2003 |
rs1136201
|
|
34
|
0.645 |
0.280 |
17 |
39723335 |
missense variant
|
A/G;T
|
snv |
0.20
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs121918080
|
|
6
|
0.827 |
0.240 |
18 |
31595128 |
missense variant
|
G/A;T
|
snv |
2.4E-05
|
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs121918090
|
|
8
|
0.790 |
0.240 |
18 |
31593026 |
missense variant
|
G/C
|
snv |
|
|
0.010 |
1.000 |
1 |
2000 |
2000 |
rs121918598
|
|
4
|
0.851 |
0.080 |
1 |
237648523 |
missense variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs12362161
|
|
3
|
1.000 |
0.040 |
11 |
98834502 |
intergenic variant
|
C/A;G
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1258130495
|
|
3
|
0.882 |
0.040 |
4 |
147485727 |
missense variant
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs12638540
|
|
1
|
1.000 |
0.040 |
3 |
32447042 |
intron variant
|
A/G;T
|
snv |
|
|
0.800 |
1.000 |
1 |
2010 |
2010 |
rs1267969615
|
|
100
|
0.532 |
0.760 |
17 |
63490960 |
missense variant
|
T/C
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
1999 |
1999 |
rs1303946678
|
|
3
|
0.925 |
0.040 |
22 |
42126851 |
missense variant
|
C/G
|
snv |
|
|
0.010 |
1.000 |
1 |
2005 |
2005 |
rs13114738
|
|
16
|
0.851 |
0.120 |
4 |
102363708 |
intron variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1337916669
|
|
2
|
0.925 |
0.040 |
6 |
26092879 |
missense variant
|
G/T
|
snv |
|
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1429117513
|
|
2
|
0.925 |
0.040 |
12 |
6775316 |
synonymous variant
|
T/C
|
snv |
4.0E-06
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1520832
|
|
1
|
1.000 |
0.040 |
12 |
42859612 |
regulatory region variant
|
T/C;G
|
snv |
|
|
0.800 |
1.000 |
1 |
2010 |
2010 |
rs1595064
|
|
2
|
0.925 |
0.040 |
2 |
211378020 |
3 prime UTR variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs1728918
|
|
19
|
0.827 |
0.160 |
2 |
27412596 |
upstream gene variant
|
A/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2016 |
2016 |
rs1799752
|
|
25
|
0.677 |
0.480 |
17 |
63488529 |
intron variant
|
-/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT
|
delins |
|
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1800624
|
|
33
|
0.658 |
0.480 |
6 |
32184610 |
upstream gene variant
|
A/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1800779
|
|
9
|
0.763 |
0.320 |
7 |
150992855 |
intron variant
|
G/A;C
|
snv |
|
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs1805192
|
|
121
|
0.510 |
0.840 |
3 |
12379739 |
missense variant
|
C/G
|
snv |
|
|
0.010 |
< 0.001 |
1 |
2019 |
2019 |