Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs972655070
TSTD1 ; USF1
0.882 0.040 1 161040282 missense variant G/A snv 4.0E-06 1.4E-05 3
rs965384857
LPL
0.827 0.160 8 19954234 missense variant G/A snv 4.0E-06 5
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5
rs9289231
KALRN
0.827 0.120 3 124055231 intergenic variant T/G snv 0.15 5
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs9267551
CLIC1 ; DDAH2
0.807 0.160 6 31730180 5 prime UTR variant C/G;T snv 7
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96 4
rs901895948
TGM2
0.882 0.040 20 38131160 missense variant C/T snv 3
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs897876 0.882 0.040 2 65564447 intron variant C/T snv 0.30 4
rs886060062
NR3C1
0.882 0.040 5 143400551 missense variant C/T snv 3
rs884164
PLIN4
0.925 0.040 19 4521613 upstream gene variant A/G;T snv 2
rs869109213
NOS3
0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113