Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs4898
TIMP1 ; SYN1 ; MIR4769
0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1555954284
DDX3X
0.752 0.360 X 41346607 missense variant C/T snv 24
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
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
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15
rs1048661
LOXL1-AS1 ; LOXL1
0.732 0.320 15 73927205 missense variant G/T snv 0.33 0.28 14
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs769217
CAT
0.742 0.440 11 34461361 synonymous variant C/T snv 0.25 0.22 12
rs7830
NOS3 ; ATG9B
0.763 0.320 7 151012483 3 prime UTR variant G/T snv 0.38 0.32 11
rs369410616
MUTYH
0.752 0.280 1 45329400 missense variant C/T snv 2.0E-05 2.8E-05 10
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs1256031
ESR2
0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 9
rs74315330
MYOCOS ; MYOC
0.776 0.080 1 171636331 missense variant G/A snv 9