Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs2867112 2 651349 intergenic variant T/G snv 0.18 3
rs12999687
DNMT3A
2 25289569 intron variant T/G snv 0.48 2
rs1320338 2 649347 intergenic variant T/G snv 0.18 2
rs149954327
STON1-GTF2A1L ; STON1
2 48582005 missense variant T/G snv 6.8E-05 1.2E-04 2
rs2440238
PAX6-AS1 ; PAUPAR
11 31886440 non coding transcript exon variant T/G snv 0.32 2
rs2867109 2 651030 regulatory region variant T/G snv 0.18 2
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs4646949
TAF11 ; UHRF1BP1
6 34877672 3 prime UTR variant T/C;G snv 3
rs8182584
PEPD
19 33418804 intron variant T/C;G snv 3
rs7574359 2 652542 intergenic variant T/C;G snv 2
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 7
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7