Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs12086634
HSD11B1-AS1 ; HSD11B1
0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs1805096
LEPR
0.827 0.200 1 65636574 synonymous variant G/A snv 0.46 0.43 6
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs7211
TXNIP
0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs142648132
MTR
0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05 5
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs2274907
ITLN1
0.851 0.200 1 160882036 missense variant A/G;T snv 0.66 5
rs5051
AGT
0.882 0.160 1 230714126 intron variant C/A;G;T snv 5
rs1514175
TNNI3K ; LRRC53 ; FPGT-TNNI3K
1.000 0.080 1 74525960 intron variant A/G snv 0.48 4
rs1800247
BGLAP ; PMF1-BGLAP
0.882 0.200 1 156242034 intron variant T/C snv 0.20 4
rs2282440
SDC3
0.882 0.240 1 30874473 missense variant G/A;C snv 9.3E-02 4
rs34603401
H6PD
0.882 0.280 1 9245386 missense variant A/C snv 0.12 0.10 4
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs397517892
LMNA
0.851 0.240 1 156136419 missense variant C/T snv 9.9E-06 1.4E-05 4
rs762403278
MTHFR
0.851 0.200 1 11796244 missense variant T/C;G snv 1.6E-05; 4.0E-06 4
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs16835198 0.882 0.200 1 32861080 downstream gene variant G/T snv 0.29 3
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3