Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800866
SIGMAR1
0.851 0.080 9 34637693 missense variant T/G snv 0.20 0.18 8
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs1531517 1.000 0.080 19 44738916 intergenic variant G/A snv 0.11 7
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 7
rs669
A2M ; KLRG1
0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 7
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 6
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs283813
NECTIN2
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16 6
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 6
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs519113
NECTIN2
1.000 0.080 19 44873027 intron variant C/G;T snv 6
rs9468
MAPT
0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 6
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 5
rs12721109
APOC4 ; APOC4-APOC2
1.000 0.080 19 44943964 intron variant G/A snv 1.3E-02 5
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs261291
ALDH1A2
1.000 0.080 15 58387979 intron variant T/A;C snv 5
rs285
LPL
1.000 0.080 8 19957678 intron variant C/T snv 0.59 5
rs28936380
PSEN2
0.827 0.080 1 226885546 missense variant C/G;T snv 1.2E-05 5
rs5112
APOC1P1
1.000 0.080 19 44927023 non coding transcript exon variant C/G snv 0.55 5
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5