Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11568819
MMP7
1.000 0.040 11 102530902 upstream gene variant G/A snv 5.5E-02 1
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs113993959
CFTR
0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 8
rs74597325
CFTR
0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 3
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 13
rs868903
MUC5B
0.882 0.120 11 1221460 upstream gene variant T/C snv 0.47 3
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 23
rs3750920
TOLLIP
0.807 0.120 11 1288726 synonymous variant C/T snv 0.40 0.38 6
rs2004640
IRF5
0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 24
rs5743890
TOLLIP
0.925 0.040 11 1304599 intron variant T/C snv 9.7E-02 4
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 18
rs2305619
VEPH1 ; PTX3
0.882 0.240 3 157437072 intron variant A/G snv 0.55 0.50 3
rs1881984 1.000 0.040 3 169746671 intergenic variant A/G snv 0.30 1
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 54
rs121917834
SFTPC
0.790 0.080 8 22163096 missense variant T/A;C snv 3.6E-05 9
rs121917835
BMP1 ; SFTPC
0.925 0.040 8 22164010 missense variant T/A snv 1
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 201
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 5
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 9
rs1043618
HSPA1L ; HSPA1A
0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 9
rs1061581
HSPA1A ; HSPA1L
0.827 0.200 6 31816809 synonymous variant G/A snv 5