Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6472903
CASC9
0.925 0.080 8 75318066 intron variant G/T snv 0.86 2
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs7558615
ERBB4
0.925 0.080 2 212081424 intron variant T/C snv 0.84 4
rs888663 0.925 0.080 19 18374112 upstream gene variant G/T snv 0.84 2
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs2494744
AKT1
0.925 0.080 14 104789477 intron variant A/G snv 0.83 2
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs1059476
AURKB
0.925 0.080 17 8205013 missense variant A/G snv 0.83 0.81 2
rs2479717
CCND3
0.925 0.080 6 41937436 intron variant T/A snv 0.79 0.81 3
rs162049
MTRR
0.925 0.080 5 7893008 non coding transcript exon variant G/A snv 0.80 2
rs10216653
CHRAC1
0.882 0.080 8 140516886 3 prime UTR variant G/C snv 0.80 3
rs425535
CXCL5
0.925 0.080 4 73998280 synonymous variant T/C snv 0.87 0.80 2
rs3003925
ESR1
0.925 0.080 6 151963323 intron variant G/A snv 0.80 2
rs1550623 0.925 0.080 2 173348166 intron variant G/A snv 0.80 2
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 6
rs1482057
RORA
0.925 0.080 15 60772552 intron variant A/C snv 0.80 2
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs2435357
RET
0.790 0.240 10 43086608 intron variant T/C snv 0.79 8
rs4704853
HAVCR2
0.925 0.080 5 157109865 intron variant A/G snv 0.79 2
rs1156287
STXBP4
0.925 0.080 17 54999438 missense variant G/A snv 0.78 0.79 2
rs805510 0.925 0.080 12 27986913 intergenic variant T/C snv 0.79 2
rs10901425
MMP21
0.851 0.200 10 125773956 missense variant A/G snv 0.76 0.78 4
rs928940
IL1RN
0.882 0.120 2 113119918 intron variant G/T snv 0.78 3