Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7939734 1.000 0.040 11 70208839 upstream gene variant T/A snv 0.57 1
rs10508293
AKR1C3
1.000 0.040 10 5098945 intron variant A/G snv 0.19 1
rs227092
ATM ; C11orf65
1.000 0.040 11 108366056 3 prime UTR variant G/A;C;T snv 1
rs17433222
C1QB
1.000 0.040 1 22652153 upstream gene variant G/A snv 0.23 1
rs10931910
AOX1
0.925 0.040 2 200659013 intron variant A/G;T snv 2
rs765669662
CA3-AS1 ; CA2
0.925 0.040 8 85465317 missense variant G/A;T snv 2.0E-05; 4.0E-06 2
rs1258094111
CTSG
0.925 0.040 14 24575388 missense variant C/T snv 4.0E-06 2
rs201820837
ETV6
0.925 0.040 12 11869532 missense variant G/A;T snv 2.4E-05; 6.4E-05 2
rs947141826
MTG1
0.925 0.040 10 133394281 missense variant C/T snv 2.1E-05 2
rs201045130
NT5C1A
0.925 0.040 1 39659467 missense variant A/G snv 9.9E-05 1.0E-04 2
rs754894156
RUNX1
0.925 0.040 21 34834544 missense variant C/T snv 4.0E-06 2
rs17886724
STAT3
0.925 0.040 17 42344145 intron variant A/G snv 0.35 2
rs703817
STAT6
0.925 0.120 12 57096045 3 prime UTR variant C/T snv 0.39 2
rs2301696
TRPM5
1.000 0.040 11 2405754 intron variant G/C snv 0.43 2
rs227060
C11orf65 ; ATM
0.882 0.160 11 108334154 intron variant C/T snv 0.27 3
rs2308950
CASP9
0.882 0.040 1 15507011 missense variant C/G;T snv 4.0E-06; 1.1E-02 3
rs6964823
IKZF1
0.925 0.040 7 50392398 intron variant G/A snv 0.45 3
rs9318227
KLF12
0.882 0.080 13 73926833 intron variant T/A;C snv 3
rs3794845
MBP
0.882 0.120 18 77002561 intron variant G/C snv 0.12 3
rs10405859
PPP1R37 ; MARK4
0.882 0.080 19 45099523 intron variant T/C snv 0.48 3
rs766274360
PRSS27
0.882 0.040 16 2713697 missense variant G/T snv 1.2E-05 3
rs139834892
XRCC1
0.882 0.040 19 43553481 missense variant C/T snv 6.4E-05 1.1E-04 3
rs974120 0.851 0.200 8 2789080 intron variant T/C;G snv 4
rs121913452
ABL1
0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs1188975135
APOBEC3C ; APOBEC3F
0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4