Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1453414
TRIM5 ; OR52N2
0.827 0.080 11 5807854 intron variant G/C;T snv 7
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 7
rs6547741
GPN1
0.807 0.080 2 27633057 intron variant G/A snv 0.53 7
rs77452476
LAMC3
0.827 0.080 9 131087186 intron variant T/G snv 0.18 7
rs79767424 0.827 0.080 5 19108581 intron variant G/T snv 4.1E-02 7
rs10462706
CLPTM1L
0.827 0.080 5 1343679 intron variant C/T snv 0.14 6
rs10851478
LOC105370811 ; FAM227B
0.827 0.080 15 49536822 intron variant T/C snv 0.30 6
rs1800628 0.827 0.080 6 31579073 downstream gene variant G/A snv 7.3E-02 6
rs2398180
NR2F2-AS1
0.827 0.080 15 96319940 intron variant C/T snv 0.62 6
rs3129780 0.827 0.080 6 32679924 intergenic variant T/A;C snv 6
rs928674
LAMC3
0.827 0.080 9 131076637 intron variant A/G snv 0.16 6
rs10090787
LOC107986874 ; SNTB1
1.000 0.080 8 120798309 intron variant C/T snv 0.34 3
rs11545028
WWOX
1.000 0.080 16 78099774 5 prime UTR variant C/T snv 0.30 0.28 3
rs2046463
LOC105377555
1.000 0.080 4 176681548 intron variant G/A;C snv 3
rs9849237
CNTN4
1.000 0.080 3 2633505 intron variant C/T snv 0.25 3
rs9862
TIMP3 ; SYN3
1.000 0.080 22 32857293 missense variant T/A;C snv 4.0E-06; 0.55 3
rs1045487
CASP8
1.000 0.080 2 201284973 synonymous variant G/A snv 9.5E-02 0.10 2
rs11130760
FHIT
1.000 0.080 3 60210809 intron variant G/T snv 0.12 2
rs1473418
BCL2
1.000 0.080 18 63319316 5 prime UTR variant C/G snv 0.98 2
rs17071138
SERPINB5
1.000 0.080 18 63476675 upstream gene variant T/C snv 2.9E-02 2
rs1950252
BCL2L2-PABPN1 ; BCL2L2
1.000 0.080 14 23309489 3 prime UTR variant A/G snv 0.93 2
rs2040639
XRCC2
1.000 0.080 7 152678103 upstream gene variant T/C;G snv 2
rs2292566
EPHX1
1.000 0.080 1 225831952 synonymous variant G/A snv 2
rs3092904
RB1
1.000 0.080 13 48477345 intron variant T/A snv 0.24 0.20 2
rs33438
ZNF536
1.000 0.080 19 30454165 intron variant G/A snv 0.50 2