Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs9138
SPP1
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs4077515
CARD9
0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 11
rs2378456
LPP
0.807 0.200 3 188885218 3 prime UTR variant C/G;T snv 6
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs12615793
ACYP2
0.851 0.280 2 54248777 intron variant G/A;T snv 4
rs3796283
LPP
0.851 0.200 3 188885163 3 prime UTR variant A/G;T snv 4
rs1056675
MPHOSPH6
0.925 0.160 16 82148329 3 prime UTR variant T/A;C snv 2
rs2364480
LTBR
0.925 0.120 12 6386109 synonymous variant C/A;T snv 0.77; 2.0E-05 2
rs2523946
HCG9 ; HLA-A
0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv 2
rs373544789
FCAR
0.925 0.120 19 54889688 missense variant G/A;T snv 8.8E-05; 3.2E-05 2
rs3795299
IL22RA1
0.925 0.200 1 24120978 missense variant G/A;C;T snv 9.6E-05; 0.42; 4.0E-06 2
rs4597342
ITGAM
0.925 0.160 16 31332448 3 prime UTR variant T/A;C snv 2
rs1008898
C1GALT1
1.000 0.120 7 7233928 intron variant G/A;T snv 1
rs11084377
FCAR
1.000 0.120 19 54875434 intron variant A/G;T snv 1
rs12716641 1.000 0.120 8 7041476 upstream gene variant T/A;C snv 1
rs1369270 1.000 0.120 2 153179546 intron variant T/C snv 1