Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs181181503
LOC100507377
0.851 0.160 12 74276187 intron variant T/C snv 1.5E-03 4
rs181997 0.925 0.160 6 32932941 downstream gene variant G/A;C snv 2
rs182123615
JAK2 ; INSL6
0.807 0.200 9 5070058 splice region variant T/C snv 3.6E-04 1.1E-03 7
rs1860661
TCF3
0.882 0.120 19 1650135 intron variant A/C;G snv 6.7E-06; 0.54 3
rs2019960
PVT1
0.925 0.160 8 128180025 intron variant T/C snv 0.27 2
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 5
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2069757
TH2LCRR
1.000 0.120 5 132662721 intron variant G/A snv 7.5E-02 1
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82