Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5996074
SREBF2
22 41840333 intron variant G/A snv 0.74 3
rs10274928
JAZF1
7 28102469 intron variant A/G;T snv 2
rs11552822
CDKN2A
1.000 9 21971109 missense variant C/A;T snv 4.3E-06 2
rs1430055 2 16499521 intergenic variant G/A snv 0.61 2
rs4851005
IL18R1
2 102395092 intron variant C/T snv 0.29 2
rs1000668
TMC1
9 72790943 intron variant T/A;G snv 1
rs10186527
FLACC1
2 201335852 intron variant C/T snv 0.54 1
rs10191793
ST6GAL2
2 106809420 intron variant A/G snv 0.21 1
rs10197246
FLACC1
2 201340018 intron variant T/C snv 0.72 1
rs10201587
FLACC1
2 201338068 intron variant A/G snv 0.47 1
rs10454127
FLACC1
2 201347651 intron variant G/A;T snv 1
rs10502995 18 55138645 regulatory region variant G/A snv 0.20 1
rs11051196
TSPAN11
12 30980130 intron variant C/T snv 0.27 1
rs11065783
LOC105369980 ; LINC01405
12 110958445 non coding transcript exon variant A/G snv 1.9E-02 1
rs11254327
CUBN
10 17006709 intron variant C/T snv 0.40 1
rs11776675
CDH17
8 94163787 intron variant T/C snv 0.23 1
rs11843987
TFDP1
13 113589954 intron variant A/G snv 9.1E-02 1
rs11898821
FLACC1
2 201334965 intron variant T/C snv 0.46 1
rs11972901 7 85966605 intergenic variant A/G snv 0.47 1
rs12438490
OCA2
15 28015163 intron variant C/T snv 7.3E-02 1
rs1323135
SDCBP2-AS1 ; FKBP1A ; FKBP1A-SDCBP2
20 1377208 non coding transcript exon variant G/C;T snv 1
rs1346291
LOC105375925
8 81339729 regulatory region variant A/G snv 0.78 1
rs1453029 18 41000207 intergenic variant T/C snv 7.0E-02 1
rs1548418
STEAP1B
7 22685795 intron variant C/A snv 0.89 1
rs1570477
KANK1
9 657340 intron variant G/A snv 0.63 1