Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 14
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs3737787
TSTD1 ; USF1
0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs1467465
THEMIS2
0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs5013329
NSUN4
0.827 0.160 1 46349419 intron variant C/T snv 0.23 6
rs638820
GSTM4 ; GSTM2
0.827 0.160 1 109667284 intron variant G/A snv 0.52 5
rs186724
AHCYL1
0.882 0.120 1 110018293 intron variant C/G;T snv 3
rs4648551
TP73
0.882 0.120 1 3716166 intron variant G/A snv 0.32 3
rs6695978
TP73
0.882 0.120 1 3731781 intron variant G/A snv 7.3E-02 3
rs7365052 0.882 0.120 1 236786561 intergenic variant T/C snv 3
rs7526063
MTR
0.882 0.120 1 236808698 splice region variant C/T snv 3.8E-02 5.6E-02 3
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs2227982
LOC105373977 ; PDCD1
0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23