Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10013040
NEIL3
1.000 0.080 4 177309998 synonymous variant C/A snv 0.20 0.20 1
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs1007888
MIF-AS1
0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 4
rs1008563 1.000 0.080 2 218162165 downstream gene variant G/A snv 0.43 1
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1012841819
ADRA2B
0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 4
rs10176176 1.000 0.080 2 85534925 upstream gene variant A/T snv 0.54 1
rs1024323
GRK4
0.882 0.160 4 3004316 missense variant C/A;G;T snv 0.36 4
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10263017
EIF2AK1
1.000 0.080 7 6026173 intron variant G/C;T snv 1
rs10281500
VOPP1
1.000 0.080 7 55475197 intron variant C/G snv 0.32 1
rs10304
SMTN ; SELENOM
0.925 0.120 22 31104550 3 prime UTR variant G/A snv 0.12 2
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10432782
SOD1
0.807 0.160 21 31664078 intron variant T/G snv 0.19 7
rs1045274
PIGQ
1.000 0.080 16 580902 synonymous variant C/G;T snv 0.16; 2.0E-05 1
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104895285
TNFRSF1A
1.000 0.080 12 6330873 missense variant A/T snv 1