rs10006235
|
|
2
|
1.000 |
0.040 |
4 |
129748953 |
non coding transcript exon variant
|
T/C
|
snv |
|
0.73
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1000731
|
|
1
|
1.000 |
0.040 |
1 |
231827745 |
intron variant
|
C/T
|
snv |
|
0.23
|
0.010 |
< 0.001 |
1 |
2018 |
2018 |
rs10012947
|
|
1
|
1.000 |
0.040 |
4 |
30491805 |
regulatory region variant
|
C/T
|
snv |
|
0.33
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs10014145
|
|
1
|
1.000 |
0.040 |
4 |
102279420 |
intron variant
|
A/G
|
snv |
|
0.31
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs10014424
|
|
1
|
1.000 |
0.040 |
4 |
99943207 |
intron variant
|
G/A
|
snv |
|
6.2E-02
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs1001684
|
|
1
|
1.000 |
0.040 |
5 |
40810324 |
intergenic variant
|
C/A
|
snv |
|
0.29
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1002424
|
|
1
|
1.000 |
0.040 |
5 |
40767295 |
intron variant
|
A/G
|
snv |
|
0.31
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs10036665
|
|
1
|
1.000 |
0.040 |
5 |
138252460 |
3 prime UTR variant
|
T/A
|
snv |
|
0.16
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs10042486
|
|
4
|
0.882 |
0.040 |
5 |
63965502 |
intron variant
|
C/T
|
snv |
|
0.58
|
0.020 |
1.000 |
2 |
2012 |
2016 |
rs10043986
|
|
2
|
0.925 |
0.040 |
5 |
79799594 |
missense variant
|
C/T
|
snv |
8.7E-02
|
8.2E-02
|
0.020 |
1.000 |
2 |
2011 |
2019 |
rs10046055
|
|
1
|
1.000 |
0.040 |
5 |
157890009 |
regulatory region variant
|
T/A
|
snv |
|
0.32
|
0.010 |
< 0.001 |
1 |
2006 |
2006 |
rs10046758
|
|
1
|
1.000 |
0.040 |
8 |
4326648 |
non coding transcript exon variant
|
C/G;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs10061788
|
|
2
|
1.000 |
0.040 |
5 |
88638889 |
intron variant
|
G/A;T
|
snv |
|
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs10063995
|
|
1
|
1.000 |
0.040 |
5 |
175445201 |
upstream gene variant
|
G/C;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs10065570
|
|
1
|
1.000 |
0.040 |
5 |
40835525 |
upstream gene variant
|
C/T
|
snv |
|
0.33
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1006737
|
|
27
|
0.695 |
0.120 |
12 |
2236129 |
intron variant
|
G/A
|
snv |
|
0.36
|
0.900 |
1.000 |
28 |
2010 |
2019 |
rs10074991
|
|
7
|
0.851 |
0.120 |
5 |
40790449 |
intron variant
|
G/A
|
snv |
|
0.31
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs10077591
|
|
1
|
1.000 |
0.040 |
5 |
165935005 |
intergenic variant
|
C/T
|
snv |
|
0.44
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs10078551
|
|
1
|
1.000 |
0.040 |
5 |
148621907 |
intron variant
|
T/C
|
snv |
|
0.26
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs1008078
|
|
2
|
1.000 |
0.040 |
1 |
90724174 |
non coding transcript exon variant
|
C/T
|
snv |
|
0.33
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs10082463
|
|
1
|
1.000 |
0.040 |
10 |
117261896 |
intron variant
|
A/C;G
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs10083370
|
|
1
|
1.000 |
0.040 |
14 |
103847845 |
intron variant
|
G/A
|
snv |
|
0.55
|
0.700 |
1.000 |
1 |
2018 |
2018 |
rs10085567
|
|
1
|
1.000 |
0.040 |
7 |
76104888 |
intron variant
|
A/C
|
snv |
|
0.43
|
0.700 |
1.000 |
1 |
2019 |
2019 |
rs1009153
|
|
1
|
1.000 |
0.040 |
15 |
22896157 |
intron variant
|
C/G;T
|
snv |
|
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs1009382
|
|
1
|
1.000 |
0.040 |
6 |
32058330 |
missense variant
|
C/A;G;T
|
snv |
0.72
|
|
0.010 |
1.000 |
1 |
2007 |
2007 |