Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs313158 6 85334045 intergenic variant A/T snv 1.8E-02 1
rs72653706
ABCC6
0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs1967309
ADCY9
0.925 0.080 16 4015582 non coding transcript exon variant A/G snv 0.51 3
rs34203073
AGGF1
1.000 0.040 5 77035624 missense variant G/A snv 1.0E-02 9.9E-03 2
rs2144151
ANGPT4
20 903001 intron variant T/G snv 0.40 1
rs749437638
ARVCF ; COMT
0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs759985000
BDNF
11 27700987 5 prime UTR variant G/A;C snv 4.2E-06; 8.4E-06 2
rs12938
C1orf112 ; SELL
0.851 0.160 1 169691640 3 prime UTR variant A/G snv 0.27 5
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs267606743
COL4A1
1.000 0.160 13 110192222 missense variant C/T snv 5
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs755460305
KNG1
0.882 0.080 3 186732650 missense variant C/A snv 4
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs6809699
P2RY12 ; MED12L
1.000 0.080 3 151338810 synonymous variant A/C snv 0.87 0.88 2
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18