Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11583706
LOC105373220
1.000 0.040 1 238358337 intron variant G/T snv 0.17 2
rs11598018
STN1
1.000 0.040 10 103901557 intron variant C/A;T snv 2
rs11599775
VTI1A
1.000 0.040 10 112699938 intron variant G/A snv 0.27 2
rs11706832
LRIG1
1.000 0.040 3 66452557 intron variant A/C;G snv 2
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2
rs12723208
TRAF5
1.000 0.040 1 211337552 intron variant A/G snv 0.13 2
rs1275600
LOC105369844
1.000 0.040 12 75869771 intron variant T/A snv 0.47 2
rs12803321
PHLDB1
1.000 0.040 11 118609400 intron variant G/C;T snv 2
rs17110757
ACOT11
1.000 0.040 1 54584133 intron variant G/A snv 0.20 2
rs2236507
RTEL1-TNFRSF6B ; RTEL1
1.000 0.040 20 63691653 intron variant G/C;T snv 2
rs4252707
MDM4
1.000 0.040 1 204539019 intron variant G/A snv 0.17 2
rs7107785
MAML2
1.000 0.040 11 96014174 intron variant T/C snv 0.57 2
rs7572263
C2orf80
1.000 0.040 2 208186862 intron variant A/G snv 0.27 2
rs77633900
ETFA
1.000 0.040 15 76246118 intron variant G/C snv 6.3E-02 2
rs8079544
TP53
1.000 0.040 17 7676734 intron variant C/T snv 7.4E-02 2
rs1673041
POLD1
19 50406132 intron variant T/A;G snv 0.73 0.79 1
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs11163687
LOC107985037
1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs12088062 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 2
rs12125049
LINC02778 ; LOC105378761
1.000 0.040 1 60202030 intergenic variant C/T snv 0.12 2
rs1409785 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 2
rs16838813 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480