Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 7
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 7
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs6504074
BRIP1
0.882 0.120 17 61822429 intron variant G/A;T snv 6
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs9389268
HBS1L
1.000 0.080 6 135098493 intron variant A/G snv 0.24 6
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs13194491 1.000 0.040 6 27069301 intergenic variant C/T snv 4.8E-02 5
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5