Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1008438
HSPA1L ; HSPA1A
0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
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
rs10159239
NLRP3
0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs1017
ISL1
1.000 0.040 5 51394261 3 prime UTR variant A/G;T snv 2
rs10217586
CDKN2B-AS1
1.000 0.040 9 22121350 intron variant A/T snv 0.52 2
rs10218795
HJV
1.000 0.040 1 146018957 intron variant G/A snv 0.15 1
rs10235849
TBX20
1.000 0.040 7 35255752 upstream gene variant T/A snv 0.36 1
rs1035071612
MIR6886 ; LDLR
0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs10420321
DNMT1
0.925 0.080 19 10189741 intron variant A/G snv 0.11 2
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
rs1042620356
GSTO1
1.000 0.040 10 104259596 missense variant A/G snv 1
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
rs10431335 1.000 0.040 12 128194523 upstream gene variant C/A;T snv 1
rs1043618
HSPA1L ; HSPA1A
0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 10