Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1408579
ERLIN1
1.000 0.040 10 100152437 intron variant C/T snv 0.32 3
rs12784396
CWF19L1
0.925 0.040 10 100267650 5 prime UTR variant C/A;T snv 4
rs7222232
GAS7
17 10033485 intron variant A/C snv 1.3E-02 2
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs17158782 5 100726979 intergenic variant T/C snv 1.9E-02 2
rs17885778
ACHE
7 100893830 missense variant G/A;C snv 4.0E-06; 1.0E-03 2
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs12097137 1 101243889 downstream gene variant G/A;T snv 3
rs2373459
SPIC
12 101480178 intron variant C/T snv 0.68 1
rs1037116 15 101528701 upstream gene variant C/T snv 0.20 2
rs10107815
MSRA
8 10156645 intron variant G/C snv 5.1E-02 4
rs6779158 3 10161878 upstream gene variant A/G snv 3.3E-02 2
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13135092
SLC39A8
4 102276925 intron variant A/G snv 5.1E-02 4
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs5742626
LINC02456 ; IGF1
12 102464131 intron variant T/C snv 2.3E-02 3
rs7001567
MSRA
8 10257027 intron variant C/G snv 3.7E-02 4
rs4648086
NFKB1 ; LOC105377347
4 102600993 missense variant G/A snv 1.6E-03 2.9E-04 2
rs5030339
LOC105372272 ; ICAM1
19 10269461 intron variant G/A snv 3.4E-03 5
rs5030361
ICAM1
19 10278833 intron variant C/T snv 6.8E-04 4
rs2075847
WTAPP1 ; MMP1
11 102799093 intron variant A/C;G snv 3
rs3025063
MMP3
11 102840709 intron variant C/T snv 2.1E-02 2
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5