Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069521 0.851 0.240 15 74746626 upstream gene variant G/A snv 4.9E-02 4
rs2278705 0.882 0.160 15 80402288 intron variant C/T snv 4.2E-02 3
rs1060499548
ABL1
0.724 0.440 9 130872961 missense variant G/A snv 27
rs10407022
AMH ; MIR4321
0.882 0.200 19 2249478 missense variant G/T snv 0.77 0.74 3
rs1114167291
ANKRD11
0.790 0.280 16 89281225 stop gained C/A snv 10
rs1364038551
AR
1.000 0.120 X 67546090 missense variant G/T snv 9.4E-06 1
rs869312712
ARID1B
0.925 0.360 6 157084866 stop gained C/T snv 3
rs1020397
ARNT2
0.882 0.160 15 80426396 intron variant G/C;T snv 3
rs5000770
ARNT2
0.882 0.160 15 80424141 intron variant G/A snv 0.27 3
rs122445099
ATRX
0.827 0.400 X 77520832 stop gained G/A snv 6
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs370681
AXIN1
0.807 0.200 16 342461 intron variant C/T snv 0.48 6
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs1554904772
BRSK2
0.882 0.280 11 1443490 missense variant G/A snv 4
rs1556425596
COL6A1
0.752 0.240 21 45989967 intron variant C/T snv 37
rs765057534
CYP19A1 ; MIR4713HG
0.851 0.240 15 51222402 missense variant C/T snv 4.0E-06 4
rs1554846212
DUPD1 ; KAT6B
0.851 0.160 10 75030037 missense variant C/T snv 9
rs1057519389
EBF3
0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs6932902
ESR1
0.882 0.160 6 152055389 intron variant G/A snv 0.22 3
rs387906692
FAM20A ; PRKAR1A
0.752 0.480 17 68530405 stop gained C/T snv 11
rs1566823361
FGF14
0.742 0.440 13 101726732 frameshift variant -/G delins 18
rs61729366
FRAS1
0.851 0.240 4 78511299 missense variant G/A snv 5.2E-03 5.8E-03 6
rs143044921
FREM2
0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 8
rs1386170575
GPR42
1.000 0.120 19 35371534 missense variant G/A snv 3.7E-05 8.5E-05 1
rs2274911
GPRC6A
0.851 0.160 6 116809541 missense variant G/A snv 0.72 0.74 6