Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs2298566
SNX19
0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs3736234
OLR1
0.851 0.040 12 10160535 non coding transcript exon variant G/A snv 0.40 4
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs4888378
CFDP1
0.851 0.040 16 75298143 intron variant A/G snv 0.52 4
rs4987262
PTGIR
0.882 0.040 19 46623592 missense variant G/A;C snv 7.1E-03 4
rs1056515
RGS5
0.882 0.040 1 163143470 3 prime UTR variant G/T snv 0.37 3
rs12347433
DELEC1 ; TNC
0.882 0.040 9 115035318 synonymous variant T/C snv 0.23 0.21 3
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3
rs212528
ECE1
0.925 0.040 1 21259168 intron variant T/C snv 0.12 3
rs2269422
AGER
0.882 0.040 6 32183517 intron variant T/C snv 1.7E-02 5.8E-03 3
rs4916251
DNM3 ; PIGC
0.882 0.040 1 172377256 intron variant T/A snv 0.70 3
rs7833904 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 3
rs79681911
SAA1
0.882 0.040 11 18269755 missense variant G/A snv 2.1E-03 8.0E-04 3
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 3
rs13447720
MRE11
0.925 0.040 11 94432160 intron variant T/C snv 0.17 2
rs138227502
ADIPOQ-AS1 ; ADIPOQ
0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04 2
rs4142986
COL15A1
0.925 0.040 9 99052344 intron variant C/A;G;T snv 1.1E-04; 0.75; 4.0E-06 2
rs4552883 0.925 0.040 8 139234730 regulatory region variant G/A;C snv 2
rs495392
KL
1.000 0.040 13 33018055 intron variant C/A snv 0.24 2
rs499952
MRE11
0.925 0.040 11 94449826 intron variant G/T snv 0.41 2