Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10488821
MPPED2
11 30480628 intron variant A/G snv 0.30 1
rs10850409 12 114943935 intergenic variant G/A snv 0.27 2
rs10853525
SETBP1
18 44856687 intron variant C/T snv 0.35 1
rs10865879
EXOG
3 38535871 intron variant A/C snv 0.21 1
rs11079159
HLF
17 55296189 intron variant A/T snv 0.25 1
rs11153730 6 118346359 intergenic variant T/C snv 0.40 4
rs11700980
N6AMT1
21 28781917 regulatory region variant T/C snv 8.7E-02 1
rs11708996
SCN5A
0.925 0.120 3 38592432 intron variant G/C snv 0.11 6
rs11710077
SCN5A
3 38616408 intron variant A/T snv 0.17 3
rs11848785
SIPA1L1
14 71590638 intron variant G/A snv 0.82 2
rs12036340 1 162045950 intergenic variant A/G snv 0.24 2
rs12039739 1 115790490 regulatory region variant C/T snv 0.28 1
rs12764182
LRMDA
10 76131488 intron variant T/G snv 0.16 1
rs12880291
SIPA1L1
14 71417850 intron variant G/T snv 0.18 1
rs13165478 5 154489480 upstream gene variant G/A snv 0.41 3
rs13185595 5 154492610 upstream gene variant G/A snv 0.41 1
rs13195040
ZNF184
1.000 0.040 6 27446145 downstream gene variant A/G snv 9.0E-02 2
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs13314892
MITF
3 69745901 intron variant A/G snv 0.23 1
rs1344852 4 20182314 intergenic variant G/A;C;T snv 1
rs1362212 7 35265695 intergenic variant G/A snv 0.11 2
rs1408224
LRCH1
13 46641083 intron variant G/A snv 0.68 1
rs1419856 7 35267372 intergenic variant A/G snv 0.11 1
rs1562782
CAND1.11 ; AMPD3
11 10321164 intron variant A/C;G snv 1
rs17020136
HEATR5B
2 37020872 intron variant T/C snv 0.24 0.18 2