Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs145611121
PRDM16
1 3402268 intron variant -/C;CC delins 1
rs770551112
ZYG11A
1 52849688 intron variant -/CT;CTT ins 1
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs4953318
PRKCE
2 46127912 intron variant A/C snv 0.43 5
rs554093579 7 100537063 upstream gene variant A/C snv 5.5E-03 1
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs1997595 21 15205839 intron variant A/C;G snv 3
rs11039436 11 47866484 intergenic variant A/C;G;T snv 2
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 11
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
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
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13 4
rs17563683
LOC107985028 ; LINC02210-CRHR1
17 45733706 intron variant A/G snv 0.15 3