Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 22
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 22
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 21
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 17
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 16
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 15
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 15
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 15
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 14