Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 100
rs2734705
CLCA1
0.925 0.120 1 86486641 missense variant A/G snv 0.86 0.87 2
rs373533
ADGRE1 ; LOC105372256
0.925 0.160 19 6919613 missense variant A/C snv 0.77 0.73 2
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs213950
CFTR-AS1 ; CFTR
0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs9300298
ADIPOR2
1.000 0.120 12 1757038 intron variant T/A snv 0.55 1
rs2228607
STX1A
0.925 0.160 7 73708593 synonymous variant A/G snv 0.51 0.53 2
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 20
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45 6
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs721917
SFTPD
0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs880633
CHI3L1
0.925 0.160 1 203183673 missense variant T/C snv 0.45 0.41 2
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs2077079
SFTPB
0.925 0.120 2 85668215 missense variant T/G snv 0.41 0.39 2
rs7512462
SLC26A9
0.882 0.200 1 205930467 intron variant T/C snv 0.38 3
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs4363087
BUD23 ; STX1A ; LOC105375350
0.925 0.160 7 73703866 3 prime UTR variant T/C snv 0.42 0.32 3
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs11003125
MBL2
0.790 0.480 10 52772254 upstream gene variant G/C snv 0.31 7
rs1124
SFTPC ; BMP1
0.882 0.160 8 22164004 missense variant G/A snv 0.30 0.26 3
rs3741156
P2RY2
1.000 0.120 11 73235095 missense variant G/A;C snv 0.29 0.20 1
rs1143639
IL1B
1.000 0.120 2 112831216 non coding transcript exon variant C/T snv 0.20 2
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 51
rs12793173
LOC102723568
0.925 0.160 11 34812657 intergenic variant T/C snv 0.18 1