Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008637
SHROOM3
4 76492991 intron variant T/A;C snv 0.35 2
rs1010553
STAB1
1.000 0.080 3 52506757 synonymous variant T/C snv 0.53 0.59 2
rs10168349
PRKCE
2 46133768 intron variant G/C snv 0.36 4
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
rs10711289
MECOM ; MECOM-AS1
3 169450583 intron variant AAA/-;A;AA;AAAA;AAAAA delins 1
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11 3
rs10953299
ACTL6B
7 100645788 intron variant T/C snv 0.21 1
rs11039436 11 47866484 intergenic variant A/C;G;T snv 2
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs11072566
NRG4
0.925 0.120 15 76001630 intron variant A/G snv 0.45 5
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs111843364
HYDIN
16 70923707 intron variant G/A snv 3.8E-02 1
rs112682076
KIF1B
1 10297748 intron variant G/C snv 5.8E-03 2
rs114948639
PRKCE
2 46066687 intron variant C/T snv 7.2E-03 3
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs11665867
SNRPA
19 40760574 intron variant A/G snv 0.13 1
rs11689538
TFCP2L1
2 121238062 intron variant G/C snv 0.11 3
rs11730623 4 69020433 upstream gene variant A/T snv 0.66 2
rs11760376 7 134684558 intron variant A/G snv 1.9E-03 2
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16