Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs267607161
TTR
0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 16
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 15
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
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs1048661
LOXL1-AS1 ; LOXL1
0.732 0.320 15 73927205 missense variant G/T snv 0.33 0.28 14
rs267607093
SRD5A3
0.851 0.160 4 55359444 stop gained G/A snv 4.0E-06 14
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs79204362
CYP1B1
0.763 0.120 2 38071251 missense variant C/T snv 5.8E-03 1.7E-03 10
rs28936700
CYP1B1 ; CYP1B1-AS1
0.776 0.120 2 38075207 missense variant C/G;T snv 5.0E-06; 3.2E-04 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
rs11258194
OPTN
0.776 0.160 10 13110400 missense variant T/A snv 4.4E-02 6.0E-02 9
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 7
rs33912345
C14orf39 ; SIX6
0.807 0.200 14 60509819 missense variant C/A;G snv 0.53 7
rs10120688
CDKN2B-AS1
0.807 0.080 9 22056500 intron variant G/A snv 0.50 7
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 7
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs3753841
COL11A1
0.827 0.080 1 102914362 missense variant G/A snv 0.61 0.49 7
rs2567206
CYP1B1 ; CYP1B1-AS1
0.827 0.200 2 38076389 non coding transcript exon variant G/A snv 0.23 7
rs28939688
OPTN
0.807 0.040 10 13109270 missense variant G/A snv 7