rs10759944
|
|
4
|
0.925 |
0.080 |
9 |
97794690 |
intron variant
|
A/G
|
snv |
|
0.72
|
0.700 |
1.000 |
3 |
2009 |
2013 |
rs1443434
|
|
4
|
0.851 |
0.080 |
9 |
97855197 |
3 prime UTR variant
|
G/T
|
snv |
|
0.63
|
0.710 |
1.000 |
2 |
2009 |
2015 |
rs1588635
|
|
2
|
1.000 |
0.080 |
9 |
97775520 |
intron variant
|
A/C
|
snv |
|
0.72
|
0.800 |
1.000 |
2 |
2010 |
2017 |
rs71369530
|
|
4
|
0.851 |
0.080 |
9 |
97854419 |
inframe insertion
|
GCCGCCGCCGCCGCCGCCGCCGCC/-;GCC;GCCGCC;GCCGCCGCC;GCCGCCGCCGCC;GCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC
|
delins |
|
0.68
|
0.020 |
1.000 |
2 |
2014 |
2014 |
rs907580
|
|
4
|
0.851 |
0.080 |
9 |
97860315 |
downstream gene variant
|
T/A;C;G
|
snv |
|
|
0.710 |
1.000 |
2 |
2009 |
2015 |
rs925487
|
|
2
|
0.925 |
0.080 |
9 |
97874116 |
regulatory region variant
|
C/A;T
|
snv |
|
|
0.700 |
1.000 |
2 |
2009 |
2013 |
rs925489
|
|
6
|
0.882 |
0.080 |
9 |
97784318 |
intron variant
|
C/T
|
snv |
|
0.71
|
0.800 |
1.000 |
2 |
2010 |
2018 |
rs10122541
|
|
1
|
1.000 |
0.080 |
9 |
97865986 |
intergenic variant
|
G/A
|
snv |
|
0.68
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs1031583860
|
|
3
|
0.882 |
0.080 |
11 |
58709815 |
missense variant
|
T/C
|
snv |
|
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1032006770
|
|
3
|
0.882 |
0.080 |
7 |
55160171 |
missense variant
|
A/G
|
snv |
4.0E-06
|
7.0E-06
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs1064795638
|
|
7
|
0.851 |
0.080 |
3 |
52403251 |
stop gained
|
G/A
|
snv |
|
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs10951937
|
|
3
|
0.882 |
0.080 |
7 |
47992027 |
intron variant
|
A/C
|
snv |
|
0.43
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs10983700
|
|
2
|
1.000 |
0.080 |
9 |
97775173 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2010 |
2010 |
rs10984103
|
|
2
|
0.925 |
0.080 |
9 |
97876993 |
TF binding site variant
|
A/C
|
snv |
|
0.68
|
0.700 |
1.000 |
1 |
2009 |
2009 |
rs1179469165
|
|
2
|
0.925 |
0.080 |
14 |
81143917 |
missense variant
|
C/T
|
snv |
8.0E-06
|
7.0E-06
|
0.010 |
1.000 |
1 |
2010 |
2010 |
rs12129938
|
|
1
|
1.000 |
0.080 |
1 |
233276815 |
intron variant
|
A/G
|
snv |
|
0.20
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs1248131654
|
|
4
|
0.851 |
0.080 |
2 |
160367217 |
missense variant
|
G/A
|
snv |
|
1.4E-05
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs12769288
|
|
3
|
0.882 |
0.080 |
10 |
129488086 |
intron variant
|
C/T
|
snv |
|
0.10
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs1365943053
|
|
3
|
0.882 |
0.080 |
9 |
95516630 |
missense variant
|
C/T
|
snv |
|
7.0E-06
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1418810723
|
|
9
|
0.851 |
0.080 |
2 |
215409981 |
missense variant
|
A/T
|
snv |
8.0E-06
|
|
0.010 |
1.000 |
1 |
2011 |
2011 |
rs1443435
|
|
1
|
1.000 |
0.080 |
9 |
97855301 |
3 prime UTR variant
|
T/C
|
snv |
|
0.63
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs1443438
|
|
8
|
0.827 |
0.080 |
9 |
97787746 |
intron variant
|
T/A;C
|
snv |
|
|
0.700 |
1.000 |
1 |
2013 |
2013 |
rs145475805
|
|
4
|
0.882 |
0.080 |
8 |
132887509 |
missense variant
|
A/G
|
snv |
8.8E-05
|
3.3E-04
|
0.010 |
1.000 |
1 |
2009 |
2009 |
rs180414
|
|
3
|
0.882 |
0.080 |
12 |
46775115 |
synonymous variant
|
A/G
|
snv |
|
3.1E-03
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs2145418
|
|
3
|
0.882 |
0.080 |
1 |
118422631 |
intergenic variant
|
C/A
|
snv |
|
0.78
|
0.010 |
1.000 |
1 |
2008 |
2008 |