Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs2300478
MEIS1
0.851 0.120 2 66554321 intron variant T/G snv 0.21 6
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs2228079
ADORA1
0.882 0.160 1 203129147 synonymous variant T/G snv 0.31 0.26 4
rs139832701
CAV3
0.925 0.080 3 8773124 intron variant T/G snv 0.13 3
rs5558
SLC6A2
0.925 0.080 16 55699647 missense variant T/G snv 3
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1491851 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs701848
PTEN
0.807 0.280 10 87966988 3 prime UTR variant T/C snv 0.33 10
rs2291738
TIMELESS
0.807 0.160 12 56421497 splice region variant T/C snv 0.43 0.39 8
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs4416670 0.827 0.240 6 43982716 intergenic variant T/C snv 0.45 7
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs10410544
SIRT2
0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 6
rs11111
GDNF-AS1 ; GDNF
0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs6903874 0.851 0.080 6 132575771 downstream gene variant T/C snv 0.23 5