Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1058261
DES
2 219420587 synonymous variant C/T snv 0.33 0.37 2
rs1058322
ADIPOR2
1.000 0.040 12 1727813 intron variant C/T snv 0.30 2
rs1058587
GDF15
0.882 0.200 19 18388612 missense variant C/G;T snv 0.24; 9.1E-06 4
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1063857
VWF
12 6044348 synonymous variant A/G snv 0.31 0.40 4
rs10740995
CACNB2
10 18156159 intron variant G/A;T snv 1
rs1074703
NCALD
8 101803258 intron variant C/A snv 0.63 1
rs10748798
PAX2
10 100794914 intron variant C/T snv 0.91 1
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs10769254
MYBPC3
11 47340914 intron variant G/C snv 0.27 4
rs10786156
PLCE1
10 94254865 intron variant C/G snv 0.44 0.47 2
rs10816914
PALM2AKAP2
9 109998608 intron variant G/A snv 0.40 1
rs10821967
RTKN2
10 62182180 downstream gene variant A/G snv 0.51 1
rs10824134
ADK
10 74261866 intron variant T/C snv 0.48 1
rs10832571
SOX6
11 16239678 intron variant C/T snv 0.16 1
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs10849891
KDM2B
12 121473799 intron variant T/A;G snv 1
rs10850407 12 114940232 intergenic variant T/G snv 0.24 1
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13