Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
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
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13