Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10046
MIR4713HG ; CYP19A1
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs10051644
CAMK2A
1.000 0.080 5 150227185 intron variant T/C snv 0.24 1
rs1007837
GAB2
1.000 0.080 11 78230030 intron variant T/C snv 0.30 1
rs10078434 1.000 0.080 5 138496342 intergenic variant A/T snv 0.13 1
rs10085109
FLT4
0.925 0.080 5 180633804 intron variant G/C;T snv 2
rs1008805
MIR4713HG ; CYP19A1
0.851 0.160 15 51257402 intron variant G/A snv 0.64 7
rs10097505
ARC
0.925 0.120 8 142612823 3 prime UTR variant G/A snv 0.47 2
rs10098778
NDUFAF6
1.000 0.080 8 94979792 intron variant C/A;T snv 1
rs1010159
SORL1
0.882 0.080 11 121612692 non coding transcript exon variant C/T snv 0.55 0.55 3
rs10109834
PTK2B
1.000 0.080 8 27354759 intron variant A/C snv 0.44 1
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 5
rs10137185
ESR2
0.925 0.200 14 64309058 intron variant C/T snv 0.17 2
rs10139154
SCFD1
0.925 0.120 14 30678292 intron variant C/T snv 0.46 2
rs10164112
STARD6
1.000 0.080 18 54355010 intron variant T/C;G snv 1
rs10173717
MTLN
1.000 0.080 2 110225473 intron variant A/G snv 0.29 1
rs10194375
BIN1
1.000 0.080 2 127082205 intron variant C/A;T snv 1
rs10207628
BIN1
0.925 0.120 2 127094445 intron variant G/A;C snv 2
rs10222981 0.925 0.080 4 6759326 upstream gene variant G/T snv 0.14 2
rs1022442 1.000 0.080 21 20983528 intergenic variant G/A snv 0.40 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1026254
MS4A4A
1.000 0.080 11 60262984 intron variant T/A;C snv 1
rs1026255
MS4A4A
1.000 0.080 11 60262476 intron variant G/A snv 0.67 1
rs1033301
VSNL1
1.000 0.080 2 17592731 intron variant A/C snv 0.11 1
rs1035071612
MIR6886 ; LDLR
0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9