Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs1126579
CXCR2
0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62 8
rs3024270
H19 ; HOTS ; MRPL23
0.776 0.200 11 1996209 non coding transcript exon variant C/G;T snv 0.46; 5.2E-06 8
rs2289278
TSLP
0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02 5
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs763569821
MUC1
0.851 0.160 1 155188197 missense variant T/C snv 1.2E-05 4
rs1126580
CXCR2
0.882 0.120 2 218136243 3 prime UTR variant G/A;T snv 3
rs3219476
MUTYH
0.882 0.200 1 45336998 intron variant A/C snv 0.58 3
rs3219472
TOE1 ; MUTYH
0.882 0.160 1 45338378 5 prime UTR variant C/T snv 0.26 3
rs2230054
CXCR2
0.925 0.080 2 218135587 synonymous variant C/T snv 0.48 0.54 2
rs1194919682
CXCR4 ; LOC112268426
0.925 0.040 2 136115158 missense variant A/G snv 2
rs7731017
DCTN4
0.925 0.080 5 150732056 intron variant T/C snv 8.3E-03 2
rs1003723
LDLR ; MIR6886
0.925 0.080 19 11113505 non coding transcript exon variant C/A;T snv 4.0E-06; 0.40 2
rs2076310
RXRB
0.925 0.080 6 33198257 intron variant A/G snv 0.27 0.28 2
rs8004738
SERPINA1
0.925 0.080 14 94390577 5 prime UTR variant G/A snv 0.55 2
rs3769839
SP110 ; SP140
0.925 0.080 2 230211910 intron variant T/C snv 0.12 2
rs761937143
SMAD4
1.000 0.040 18 51047229 synonymous variant A/C snv 8.0E-06 1