Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs2165241
LOXL1-AS1 ; LOXL1
0.716 0.360 15 73929861 intron variant T/C snv 0.60 15
rs3825942
LOXL1 ; LOXL1-AS1
0.716 0.320 15 73927241 missense variant G/A;C;T snv 0.18; 4.5E-06 15
rs74315329
MYOC ; MYOCOS
0.732 0.240 1 171636338 stop gained G/A snv 1.1E-03 8.7E-04 15
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs11258194
OPTN
0.776 0.160 10 13110400 missense variant T/A snv 4.4E-02 6.0E-02 9
rs10120688
CDKN2B-AS1
0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs28939688
OPTN
0.807 0.040 10 13109270 missense variant G/A snv 7
rs199746824
MYOC
0.807 0.040 1 171652139 missense variant C/G;T snv 4.0E-06; 1.6E-05 6
rs1900004
LINC02640
0.827 0.040 10 68241124 intron variant C/T snv 0.39 5
rs2274755
MMP9
0.882 0.040 20 46011053 splice region variant G/T snv 0.15 0.15 5
rs10483727 0.851 0.040 14 60606157 upstream gene variant T/C snv 0.45 4
rs4236601 0.882 0.040 7 116522675 upstream gene variant G/A snv 0.28 4